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A case of ulnar nerve section at the elbow alleviated by Martin-Gruber communicating branch. Diagnostic characterization

Hand surgery and rehabilitation, 2022-04, Vol.41 (2), p.270-272

2022

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A new severe mutation in the SLC5A7 gene related to congenital myasthenic syndrome type 20

Neuromuscular disorders : NMD, 2018-10, Vol.28 (10), p.881-884

2018

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A series of patients with refractory myasthenia gravis

Neurología (Barcelona, English ed. ), 2023-05

2023

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Ocular myasthenia gravis and risk factors for developing a secondary generalisation: Description of a Spanish series

Neurología (Barcelona, English ed. ), 2023-05

2023

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A new case of the absence of N20 at early cerebral anoxia-ischemia evaluation by somatosensory evoked potentials

Medicina intensiva, 2014-04, Vol.38 (3), p.194

2014

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Cranial polyneuritis related to varicella-zoster virus infection. A case report

Revue neurologique, 2022-04, Vol.178 (4), p.401-403

2022

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Carpal tunnel syndrome. The contribution of ultrasonography

Revista de neurologiá, 2014-11, Vol.59 (10), p.459-469

Pardal-Fernandez, J M

2014

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A new median motor test: comparison with conventional motor studies in carpal tunnel syndrome

Journal of clinical neurophysiology, 2012-02, Vol.29 (1), p.84-88

2012

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Satoyoshi's syndrome related muscle spasms: Functional study

Revue neurologique, 2012-03, Vol.168 (3), p.291-295

2012

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Congenital gingival hyperplasia in a neonate with foetal valproate syndrome

Neuropediatrics, 2007-10, Vol.38 (5), p.251-252

2007

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Lumbar radiculopathy associated with focal denervation hyperhidrosis

Revue neurologique, 2014-01, Vol.170 (1), p.54-55

2014

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Spanish family with spastic paraplegia and demyelinating polyneuropathy: a disease related with PLP1 null syndrome

Revista de neurologiá, 2012-12, Vol.55 (12), p.765-765

Pardal-Fernandez, J M

2012

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Considerations on the negative electroretinogram

Archivos de la Sociedad Española de Oftalmología (English ed.), 2018-07, Vol.93 (7), p.e45-e46

2018

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G.P.17.02 New c-terminal titin mutations in Europeans with tibial muscular dystrophy (TMD)

Neuromuscular disorders : NMD, 2007, Vol.17 (9), p.884-884

2007

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A 2.84 Mb deletion at 21q22.11 in a patient clinically diagnosed with marden-walker syndrome

American journal of medical genetics. Part A, 2013-09, Vol.161A (9), p.2281-2290

2013

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Lepra neural pura. Aspectos diagnósticos en un caso clínico

Revista de neurologiá, 2016-09, Vol.63 (6), p.257

2016

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Pure neural leprosy. Diagnostic aspects of a clinical case

Revista de neurologiá, 2016-09, Vol.63 (6), p.257-261

2016

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Value of electroencephalography in the early detection of neonatal leucinosis

Revista de neurologiá, 2016-08, Vol.63 (4), p.160

2016

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Pena-Shokeir syndrome type I, associated to Klippel-Feil syndrome type II in the same family

Revista de neurologiá, 2007-08, Vol.45 (4), p.229-232

2007

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Diagnosis and treatment in a case of respiratory myoclonus

Revista de neurologiá, 2006-12, Vol.43 (11), p.699

2006

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Hypertrophie neurogène au cours d'une radiculopathie L5

Revue neurologique, 2011, Vol.167 (6-7), p.545-546

2011

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Denervation hypertrophy in L5 radiculopathy

Revue neurologique, 2011-06, Vol.167 (6), p.545-546

2011

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Tonic vasomotor control by the rostral ventrolateral medulla: effect of electrical or chemical stimulation of the area containing C1 adrenaline neurons on arterial pressure, heart rate, and plasma catecholamines and vasopressin

The Journal of neuroscience, 1984-02, Vol.4 (2), p.474-494

1984

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Chronic relapsing axonal neuropathy. A case report

Revista de neurologiá, 2005-11, Vol.41 (10), p.596-600

2005

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Embryopathy due to valproic acid with severe malformations in the central nervous system

Revista de neurologiá, 2006-03, Vol.42 (6), p.336

2006

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A case of ulnar nerve section at the elbow alleviated by Martin-Gruber communicating branch. Diagnostic characterization

A new severe mutation in the SLC5A7 gene related to congenital myasthenic syndrome type 20

A series of patients with refractory myasthenia gravis

Ocular myasthenia gravis and risk factors for developing a secondary generalisation: Description of a Spanish series

A new case of the absence of N20 at early cerebral anoxia-ischemia evaluation by somatosensory evoked potentials

Cranial polyneuritis related to varicella-zoster virus infection. A case report

Carpal tunnel syndrome. The contribution of ultrasonography

A new median motor test: comparison with conventional motor studies in carpal tunnel syndrome

Satoyoshi's syndrome related muscle spasms: Functional study

Congenital gingival hyperplasia in a neonate with foetal valproate syndrome

Lumbar radiculopathy associated with focal denervation hyperhidrosis

Spanish family with spastic paraplegia and demyelinating polyneuropathy: a disease related with PLP1 null syndrome

Considerations on the negative electroretinogram

G.P.17.02 New c-terminal titin mutations in Europeans with tibial muscular dystrophy (TMD)

A 2.84 Mb deletion at 21q22.11 in a patient clinically diagnosed with marden-walker syndrome

Lepra neural pura. Aspectos diagnósticos en un caso clínico

Pure neural leprosy. Diagnostic aspects of a clinical case

Value of electroencephalography in the early detection of neonatal leucinosis

Pena-Shokeir syndrome type I, associated to Klippel-Feil syndrome type II in the same family

Diagnosis and treatment in a case of respiratory myoclonus

Hypertrophie neurogène au cours d'une radiculopathie L5

Denervation hypertrophy in L5 radiculopathy

Tonic vasomotor control by the rostral ventrolateral medulla: effect of electrical or chemical stimulation of the area containing C1 adrenaline neurons on arterial pressure, heart rate, and plasma catecholamines and vasopressin

Chronic relapsing axonal neuropathy. A case report

Embryopathy due to valproic acid with severe malformations in the central nervous system

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