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H-reflex

The H-reflex, also known as the Hoffmann reflex, is an electrically induced monosynaptic reflex that serves as a physiological analog to the mechanically elicited spinal stretch reflex, allowing direct assessment of Ia afferent-to-alpha motoneuron synaptic transmission in the spinal cord.^[1] It is elicited by low-intensity percutaneous electrical stimulation of a mixed peripheral nerve, such as the posterior tibial nerve for the soleus muscle, which selectively activates group Ia muscle spindle afferents and bypasses the muscle spindle itself to produce a measurable electromyographic response in the target muscle.^[1] First described by German physiologist Paul Hoffmann in 1910, the H-reflex has become a cornerstone tool in neurophysiology for evaluating spinal excitability, nerve conduction across proximal segments like roots and plexuses, and central modulation of reflexes.^[1] The H-reflex pathway mirrors the stretch reflex circuit and is modulated by various inhibitory and excitatory mechanisms, with its amplitude reflecting motoneuron pool excitability. It finds applications in diagnosing neuromuscular disorders, assessing motor control, and facilitating rehabilitation through techniques like operant conditioning to promote spinal plasticity.^[2]^[3]

Physiology

Definition and Basic Mechanism

The H-reflex, also known as the Hoffmann reflex, is an electrically elicited monosynaptic reflex that serves as an analog to the mechanically induced stretch reflex. It is evoked by submaximal electrical stimulation of Ia afferent fibers within a mixed peripheral nerve, producing a biphasic response on electromyography (EMG). This response includes an early M-wave, representing the direct activation of motor axons with a latency of approximately 3–6 ms, followed by a later H-wave, which reflects the reflex activation of motor neurons with a latency of about 28–35 ms in lower limb muscles such as the soleus and shorter latencies (around 17–20 ms) in upper limb muscles like the flexor carpi radialis.^[4]^[5]^[1] The core mechanism of the H-reflex bypasses the muscle spindle's mechanical stretch by directly stimulating Ia afferent fibers originating from muscle spindles. These afferents form monosynaptic connections with alpha motor neurons in the spinal cord, leading to excitatory postsynaptic potentials that trigger a reflex muscle contraction. The amplitude of the H-wave provides a measure of the excitability of the spinal motoneuron pool, as it depends on the number of motor neurons recruited by the afferent volley.^[6] As stimulus intensity increases from submaximal levels, the H-reflex amplitude initially rises due to recruitment of more Ia afferents but subsequently decreases because of collision between the orthodromic (reflex) volley traveling toward the muscle and the antidromic (back-propagating) motor volley from direct axon activation. At supramaximal intensities, the H-wave is extinguished entirely, overwhelmed by the maximal M-wave, which reflects full activation of motor axons. This stimulus-response dynamic underscores the H-reflex's utility as a quantifiable electrical counterpart to the ankle jerk reflex, enabling precise evaluation of spinal reflex excitability without mechanical perturbation.^[2]^[1]

Neural Pathway and Reflex Arc

The neural pathway of the H-reflex begins with electrical stimulation of Ia afferent fibers within a peripheral nerve, such as the tibial nerve for the soleus muscle H-reflex. These Ia fibers, originating from muscle spindle primary endings, conduct action potentials orthodromically to the dorsal horn of the spinal cord, typically at the L5-S1 segments for lower limb reflexes. Upon entering the spinal cord, the Ia afferents synapse directly onto alpha motor neurons located in the ventral horn, forming a monosynaptic connection that bypasses interneurons in the primary pathway.^[7]^[8] The reflex arc encompasses both afferent and efferent components, with the incoming Ia signals triggering excitation of alpha motor neurons, whose axons then exit via the ventral root to reinnervate the target muscle, generating the H-wave on electromyography. A key modulatory element is primary afferent depolarization (PAD), mediated by GABAergic interneurons that depolarize the central terminals of Ia afferents, leading to presynaptic inhibition that reduces transmitter release and reflex amplitude. The basic H-reflex arc operates entirely at the spinal level without supraspinal involvement, although descending pathways can modulate it during voluntary movement.^[7]^[9] The monosynaptic nature of the H-reflex is evidenced by its consistent latency, reflecting the direct Ia-to-motoneuron linkage without interneuronal delays, and the absence of interneurons in the core pathway. This allows estimation of Ia afferent conduction velocity (CV) using the formula:

CV = \frac{d}{t_H - t_M}

where CV is in m/s, d is the distance from stimulation site to spinal cord entry in meters, t_H is the H-reflex latency in seconds, and t_M is the M-wave latency in seconds; this calculation verifies involvement of fast-conducting Ia fibers by isolating the afferent conduction time (t_H - t_M approximates the time for the Ia afferent signal to travel to the spinal cord plus synaptic delay).^[10] The H-reflex is absent or reduced in conditions affecting the Ia-motoneuron synapses, such as peripheral neuropathies that impair Ia fiber conduction or synaptic transmission.^[7]

Measurement Techniques

Stimulation and Recording Methods

Stimulation of the H-reflex typically employs a constant-current electrical stimulator that delivers square-wave pulses with a duration of 0.1 to 1 ms and intensities ranging from 10 to 50 mA.^[1] These pulses are applied via surface electrodes positioned over the target nerve, such as the posterior tibial nerve in the popliteal fossa for the soleus muscle or the median nerve at the elbow for the flexor carpi radialis (FCR).^[2] To optimize the H-wave while minimizing interference from the direct M-wave, stimulation intensity is set to a submaximal level, often 20-50% of that required to elicit the maximum M-wave (M-max).^[1] Recording of the H-reflex involves surface electromyography (EMG) electrodes placed in a belly-tendon montage over the target muscle, such as the soleus, with the active electrode on the muscle belly and the reference on the tendon, spaced approximately 2 cm apart.^[11] The electrodes connect to an EMG amplifier with a bandpass filter of 10-5000 Hz and a gain of 100-1000 µV to capture the evoked potentials clearly.^[11] Signals are digitized at a sampling rate exceeding 2 kHz for accurate waveform analysis, and the H/M ratio is computed as the peak-to-peak amplitude of the H-wave divided by that of the M-wave to normalize for motoneuron pool excitability.^[1] Standard protocols utilize single-pulse or paired-pulse stimulation delivered at intervals of at least 10 seconds to prevent post-activation depression, with 10-20 trials averaged to reduce background noise and enhance signal reliability.^[1] Safety protocols emphasize currents below 50 mA to avoid skin burns or cardiac interference, along with low stimulation rates (0.3-1 Hz at rest) to minimize subject discomfort.^[2] Recent advancements include multiplexed recording devices, such as a 2025 compact signal distributor with 10 output channels, enabling simultaneous H-reflex elicitation and capture from multiple muscles to improve clinical efficiency and reduce variability from sequential testing.^[12]

Factors Affecting H-reflex Amplitude

The amplitude of the H-reflex is modulated by a variety of intrinsic and extrinsic factors that influence the excitability of the spinal reflex arc, necessitating careful control in experimental and clinical assessments to ensure reliable interpretation. Intrinsic factors primarily involve neural mechanisms within the reflex pathway, while extrinsic factors encompass biomechanical and environmental influences. These modulations highlight the sensitivity of the H-reflex to physiological context, affecting its utility as a probe of spinal excitability. Post-activation depression, also known as rate-dependent depression, is a key intrinsic factor where repeated stimulation of Ia afferents leads to a progressive reduction in H-reflex amplitude due to presynaptic inhibition of Ia terminals. This phenomenon is evident at stimulation frequencies of 1-5 Hz, with H-reflex suppression reaching approximately 67% at 1 Hz and 88% at 5 Hz in healthy individuals, reflecting mechanisms such as neurotransmitter depletion and enhanced primary afferent depolarization. An empirical model describes this decay as an exponential function, where the ratio of the nth H-reflex amplitude to the first (H_n / H_1) approximates e^(-k × (n-1)), with k representing the depression constant and n the pulse number in paired or train stimuli. Background electromyographic (EMG) activity represents another intrinsic modulator, where increasing voluntary contraction facilitates the motor neuron pool, leading to a linear rise in H-reflex amplitude proportional to the level of ongoing muscle activation. This enhancement occurs through heightened excitatory drive to motoneurons, independent of changes in presynaptic inhibition. Extrinsic factors include muscle length and tension, which alter Ia afferent sensitivity and reflex gain; the H-reflex amplitude is typically larger at shortened muscle lengths compared to stretched positions, as lengthening increases post-activation depression and recurrent inhibition, thereby suppressing reflex responses. Environmental conditions such as microgravity also exert significant effects, with H-reflex excitability decreasing by about 35% shortly after exposure to weightlessness during space missions, as observed in studies aboard the International Space Station, and recovering to baseline within 10 days post-return. Cutaneous inputs provide a specific example of sensory modulation, where pressure applied to the Achilles tendon via circumferential compression at 40-45 mmHg reduces unconditioned H-reflex amplitude by approximately 55%, an effect attributed to presynaptic inhibition of Ia afferents that reverses within one minute after pressure release. Age-related changes contribute to a progressive decline in H-reflex amplitude, with the H/M ratio decreasing by about 1-2% per decade after age 30, primarily linked to motoneuron loss and reduced spinal excitability. This decline manifests as lower maximal H-reflex responses relative to the direct muscle response (M-wave), underscoring the impact of neural remodeling on reflex integrity in older adults.

Clinical and Research Applications

Diagnostic Uses in Neuromuscular Disorders

The H-reflex serves as a valuable electrophysiological tool in diagnosing neuromuscular disorders by assessing the integrity of the Ia afferent-motoneuron monosynaptic pathway, particularly in the soleus muscle, where abnormalities such as reduced amplitude or absence indicate proximal lesions like S1 radiculopathy or peripheral neuropathy.^[13] In S1 radiculopathy, a reduced or absent H-reflex reflects disruption at the nerve root level, while in peripheral neuropathies, such as diabetic polyneuropathy, the H/M ratio often falls below normal thresholds, signifying axonal loss or conduction slowing.^[14] Prolonged H-reflex latency exceeding approximately 35 ms (normal range ~25-35 ms, mean 28-31 ms, adjusted for height and age), suggests demyelination, as seen in Guillain-Barré syndrome, where early absence or delay of the reflex correlates with proximal nerve involvement.^[15]^[16] In spinal cord injury (SCI), H-reflex testing reveals distinct patterns across phases; post-acute hyperactivity, marked by an elevated H/M ratio, indicates spasticity due to loss of descending inhibition and enhanced motoneuron excitability below the lesion.^[17] This elevation in H-reflex amplitude reflects spinal disinhibition, aiding in quantifying spasticity severity. In amyotrophic lateral sclerosis (ALS), alterations in H-reflex excitability, such as increased H/M ratios or absence, correlate with progressive motoneuron degeneration, providing an early marker of lower motor neuron involvement before overt clinical weakness.^[18] Bilateral H-reflex testing enhances early detection of lumbosacral radiculopathy, with side-to-side amplitude asymmetry serving as an early indicator of nerve root involvement.^[14] A 2020 systematic review highlights the prognostic utility of the H-reflex in traumatic SCI for monitoring motor recovery and spasticity.^[19] Threshold values for interpretation include a normal H/M ratio of 0.3-0.7 in the soleus muscle at rest, reflecting balanced motoneuron pool excitability; ratios below 0.3 suggest afferent or efferent pathway compromise, while asymmetry exceeding 20% in amplitude indicates unilateral pathology, such as radiculopathy.^[20] These metrics, derived from standardized stimulation protocols, allow clinicians to differentiate central from peripheral lesions when integrated with nerve conduction studies.^[21]

Applications in Motor Control and Rehabilitation

The H-reflex serves as a key tool in motor control research to evaluate dynamic changes in spinal excitability during locomotion. In healthy individuals, soleus H-reflex amplitude is phase-dependently modulated, with notable depression during the early stance and swing phases of gait, primarily attributed to presynaptic inhibition of Ia afferents.^[22]^[23] This modulation reflects adaptive spinal mechanisms that optimize muscle activation for efficient movement. A 2022 review highlights the H-reflex's role in probing central pattern generator (CPG) modulation, demonstrating how afferent feedback integrates with spinal networks to fine-tune locomotor rhythms in humans.^[24] In rehabilitation, H-reflex conditioning protocols, including biofeedback-based operant training, have been applied to normalize reflex excitability in stroke survivors, targeting spasticity reduction through targeted downregulation of the soleus H-reflex. These interventions promote functional recovery by enhancing voluntary control and decreasing hyperreflexia, with studies showing significant improvements in motor function over training periods.^[25]^[26] In aging populations, H-reflex measurements track neuromuscular adaptations to resistance training, where increases in the H/M ratio indicate enhanced spinal motoneuron excitability and strength gains, supporting interventions to counteract sarcopenia-related declines.^[27] Recent advancements include 2024 studies on rate-dependent depression (RDD) of the H-reflex, which reveal impaired spinal inhibitory mechanisms in diabetic neuropathy, offering a biomarker for monitoring disease progression and potential links to glycemic control through early detection of sensory-motor deficits.^[28] In sports medicine, post-fatigue H-reflex modulation provides insights into recovery dynamics, with persistent alterations in reflex excitability correlating to extended restoration timelines after intense exercise.^[29] Additionally, H-reflex assessments in simulated microgravity environments have demonstrated stable reflex responses, unaffected by acute exposure to altered gravity.^[30]

History and Development

Discovery and Early Studies

The H-reflex was first described by German physiologist Paul Hoffmann in 1918 through experiments involving electrical stimulation of human nerves, such as the tibial nerve, where he observed a late reflex wave distinct from the direct muscle response, which he termed the "Hoffmann wave."^[31] This finding was reported in his seminal paper "Über die Beziehungen der Sehnenreflexe zur willkürlichen Bewegung und zum Tonus," published in Zeitschrift für Biologie, highlighting the reflex's role in tendon responses and its potential analogy to stretch reflexes.^[32] Hoffmann's work built on his earlier 1910 studies of human reflexes but provided the foundational electrical elicitation method for the specific late-wave observation.^[2] The reflex was more systematically confirmed in humans by John W. Magladery and David B. McDougal Jr. in 1950, who elicited it in the soleus muscle through submaximal electrical stimulation of the posterior tibial nerve, identifying it as an electrically evoked counterpart to the ankle jerk reflex.^[33] Their studies, published in the Bulletin of the Johns Hopkins Hospital, established key electromyographic (EMG) characteristics, including the reflex's latency and amplitude dependence on stimulus intensity.^[33] In the 1950s, experiments further validated the H-reflex's monosynaptic nature in humans through latency measurements—typically 28-32 ms for the soleus—and collision techniques, where orthodromic and antidromic impulses interfered, confirming a single synaptic delay akin to animal models.^[34] These methods, advanced by Magladery and collaborators, demonstrated the reflex's reliance on Ia afferent fibers synapsing directly onto alpha motoneurons.^[33] Post-World War II advancements in EMG technology, including improved amplifiers and recording electrodes, facilitated routine human H-reflex testing by the 1960s, shifting the focus from animal preparations to clinical and physiological applications in awake subjects.^[1]

Advancements in Methodology

In the 1970s, advancements in H-reflex methodology focused on normalizing reflex measurements to account for variations in motoneuron pool excitability and peripheral factors during voluntary contractions. Upton et al. introduced the H/M ratio as a key metric, where the amplitude of the maximum H-reflex (H_max) is divided by the maximum M-wave (M_max) amplitude, enabling more reliable comparisons across conditions and subjects by mitigating influences like electrode placement or stimulus intensity fluctuations. This normalization technique became widely adopted for assessing spinal excitability in active states, building on earlier passive reflex studies. The 1980s saw the development of paired-stimulus paradigms to investigate inhibitory mechanisms, particularly presynaptic inhibition and homosynaptic depression. By delivering two closely spaced stimuli to elicit a first H-reflex (H1) followed by a second (H2), researchers quantified depression as the H2/H1 ratio, revealing frequency-dependent reductions in Ia afferent efficacy that reflect central spinal modulation. These methods, exemplified in studies of voluntary movement onset, provided insights into dynamic reflex suppression without relying on single-pulse variability.^[24] Concurrently, the 1990s marked a shift from invasive needle electrodes for recording to non-invasive surface electromyography (EMG), enhancing clinical accessibility and reducing patient discomfort while maintaining signal fidelity for routine testing.^[1] Entering the 2000s, digital signal processing techniques revolutionized H-reflex analysis by improving noise reduction and artifact rejection through advanced filtering and averaging algorithms. These computational methods allowed for clearer isolation of reflex components in noisy environments, such as during locomotion or multi-muscle recordings, surpassing analog limitations of prior decades. A 2006 methodological review by Stein and Thompson emphasized strategies for stimulus artifact minimization, including optimized electrode configurations and timing adjustments, which further refined reliability in experimental settings.^[35] Recent developments in the 2020s have integrated H-reflex protocols with transcranial magnetic stimulation (TMS) to probe corticospinal-spinal interactions in motor control. A 2022 review highlighted how concurrent TMS-H-reflex paradigms reveal supraspinal influences on reflex gain, aiding studies of balance and adaptation in healthy and impaired populations.^[36] By 2025, multiplexed EMG devices facilitated simultaneous multi-site H-reflex testing across large cohorts, supporting population-level analyses of spinal excitability variations in sports science and rehabilitation.^[12]

References

[1]
The Hoffmann Reflex: Methodologic Considerations and ... - NIH
The Hoffmann reflex (H-reflex) is an electrically induced reflex analogous to the mechanically induced spinal stretch reflex.
[2]
Clinical uses of H reflexes of upper and lower limb muscles - PMC
Perhaps the major use for H reflex studies is that they allow the clinician to study conduction across proximal segments (i.e., plexuses and nerve roots) of ...Missing: neuroscience | Show results with:neuroscience
[3]
Soleus H-reflex gain in humans walking and running under ...
The Hoffmann (H-) reflex is an electrical analogue of the monosynaptic stretch reflex, elicited by bypassing the muscle spindle and directly stimulating the ...
[4]
H-Reflex Up-Conditioning Encourages Recovery of EMG Activity ...
Dec 1, 2010 · Operant conditioning of the spinal stretch reflex or its electrical analog, the H-reflex, produces spinal cord plasticity and can thereby affect ...
[5]
Evaluation of the relation between triceps surae H-reflex, M ...
We found a significant correlation between H-reflex latency and M-latency (r ... The mean M-response latency was 4.17 ± 0.63 msec with range of 3-6 msec.
[6]
The H-reflex study of the flexor carpi radialis muscle in healthy ... - NIH
Nov 19, 2024 · Normative values for the upper limit of latency range from 17 to 19 ms (17, 20, 21). However, multiple regression analyses show that latency ...
[7]
Monosynaptic Reflex - StatPearls - NCBI Bookshelf - NIH
Sep 12, 2022 · The Hoffmann reflex, or "H reflex," is similar to the muscle stretch reflex and is elicited through selective electrical stimulation of the ...
[8]
H-reflex to S1-root stimulation improves utility for diagnosing S1 ...
The H-reflex on stimulation of the tibial nerve in the popliteal fossa is routinely used in the diagnosis of first sacral (S1) nerve-root radiculopathy.
[9]
Post‐activation depression from primary afferent depolarization ...
Mar 16, 2023 · Post-activation depression from primary afferent depolarization (PAD) produces extensor H-reflex suppression following flexor afferent conditioning.
[10]
None
### Conduction Velocity Estimation Formula for Ia Fibers in H-Reflex
[11]
Reliability of the Soleus H-Reflex in Different Sitting Postures - NIH
Nov 25, 2020 · The Soleus (SOL) Hoffmann reflex (H-reflex) is commonly recorded in sitting position. However, the reliability of recording is unknown.2.3. Experimental Procedure · 2.4. Statistical Analysis · Table 2
[12]
H-reflex to S1-root stimulation improves utility for ... - PubMed
Thus, H-reflex to S1-root stimulation significantly increases the diagnostic sensitivity for S1 radiculopathy. Significance: In our study, the S1-root H-reflex ...
[13]
H-reflex amplitude asymmetry is an earlier sign of nerve root ...
Apr 5, 2011 · H-reflex amplitude asymmetry is an earlier sign/parameter of nerve root involvement in patients with radiculopathy compared with latency.
[14]
H-Reflex - an overview | ScienceDirect Topics
Finally, the H reflex latency (and often amplitude) is constant when elicited by the same stimulus intensity, since it reflects activation of the same motor ...
[15]
H-reflex changes following spinal cord injury - PubMed
The monosynaptic H-reflex to the triceps surae muscles was tested serially over the first six months after traumatic spinal cord injury (SCI).
[16]
A Study of H reflex in amyotrophic lateral sclerosis. - Neurology India
In amyotrophic lateral sclerosis (ALS), both anterior horn cell and corticospinal tracts are affected. H reflex studies were performed in 15 patients to ...
[17]
H-reflex as an Outcome Measure in Individuals with Spinal Cord Injury
May 21, 2024 · It showed that the H-reflex can be a useful tool in evaluating the prognosis, as it assess the excitability below the level of injury.
[18]
Hoffmann Reflex - an overview | ScienceDirect Topics
The H/M ratio for calf H reflexes is normally less than 0.7 but there is considerable variation. A recent study has recommended evaluating M responses and H ...Missing: per decade
[19]
H-reflex amplitude asymmetry is an earlier sign of nerve root ...
H-reflex amplitude asymmetry is an earlier sign/parameter of nerve root involvement in patients with radiculopathy compared with latency.
[20]
Excitability of the soleus H-reflex arc during walking and stepping in ...
During bipedal treadmill walking, excitability was decreased in the early stance, maximally enhanced in the second half of the stance, and again decreased ...
[21]
Soleus H-reflex Excitability Changes in Response to Sinusoidal Hip ...
The soleus H-reflex is modulated during human locomotion in a phase-dependent manner, so it is depressed at early stance and during the swing phase, while it ...
[22]
Revisiting the use of Hoffmann reflex in motor control research on ...
Dec 26, 2022 · This brief narrative review discusses the purpose of the H reflex and emphasizes its use as a tool to assess the effectiveness of Ia afferents in discharging ...
[23]
Exercise induced operant conditioning of the H-reflex in stroke patients
Conclusion. The results suggest that stroke patients have the ability to down-regulate the Hreflex amid corticospinal damages.Abstract · Introduction · Method · Results
[24]
Reducing the Soleus Stretch Reflex With Conditioning - Frontiers
Operant conditioning of the reflex response is a promising, non-invasive paradigm to obtain a long-term spasticity reduction (4, 5). Within the conditioning ...
[25]
Neural adaptation to resistance training: changes in evoked V-wave ...
... H-reflex amplitude gradually decreases because of the increase in antidromic collision (C and D). At a given stimulus intensity, an elevated H-reflex ...
[26]
Rate-Dependent Depression of the Hoffmann Reflex - PubMed Central
Nov 21, 2024 · RDD, a modified H-reflex technique, is widely used to assess movement disorders. RDD is impaired in rodents and some humans with painful DPN.
[27]
Changes in H-reflex, V-wave, and contractile properties of the ...
The H-reflex is a useful probe to examine neural adaptations at the spinal level, reflecting the transmission of reflexes between Ia afferent neurons and ...
[28]
Acute exposure to microgravity does not influence the H-reflex with ...
Therefore, the purpose of the study was to compare Ia afferent transmission in microgravity and NG and to assess how microgravity affects muscle activity during ...
[29]
Hoffmann Reflex - an overview | ScienceDirect Topics
Hoffmann first described the H-reflex in 1918. Traditionally, this response has been considered the electrophysiologic equivalent of the Achilles' tendon muscle ...
[30]
Central control of reciprocal inhibition during fictive dorsiflexion in man
Hoffmann P (1918) Über die Beziehungen der Sehnenreflexe zur willkürlichen Bewegung. Zeitschrift für Biologie 68: 351–370. Google Scholar. Hultborn H, Meunier ...
[31]
CALIBRE SPECTRA OF MOTOR AND SENSORY NERVE FIBRES ...
Published Online:01 Mar 1948https://doi.org/10.1152/jn.1948.11.2.133 ... Populations of motor units of the human soleus muscle supplying H reflex generation: ...
[32]
Electrophysiological studies of nerve and reflex activity in ... - PubMed
Identification of certain reflexes in the electromyogram and the conduction velocity of peripheral nerve fibers. Bull Johns Hopkins Hosp. 1950 May;86(5):265-90.Missing: H- | Show results with:H-
[33]
https://pubmed.ncbi.nlm.nih.gov/15414383/
[34]
Neural Plasticity in Spinal and Corticospinal Pathways Induced by ...
The soleus H-reflex and the single-pulse, subthreshold, TMS-evoked MEP in the soleus were timed to arrive during the short (SLR) or long-latency response (LLR) ...
[35]
Wireless Soft Athlete Bioelectronics for Monitoring Carbon Dioxide ...
Jun 20, 2025 · Here, a wireless soft athlete bioelectronic system is presented that monitors various physiological signals and metabolites during exercise.
[36]
The Multiplexed Device for Hoffmann Reflex Detection - 2025
Apr 23, 2025 · The multichannel H-reflex technique involves recording H-reflexes from multiple muscles or different sites within the same muscle simultaneously ...