Warning: Undefined array key "mm" in /www/wwwroot/www.ai-bt.com/si.php on line 10 Deprecated: trim(): Passing null to parameter #1 ($string) of type string is deprecated in /www/wwwroot/www.ai-bt.com/si.php on line 10 Peroneal muscular atrophy (PMA) and related disorders. I. Clinical manifestations as related to biopsy findings, nerve conduction and electromyography.

× No keyword cloud information.

33 in total

1. Hereditary motor and sensory neuropathy type II (HMSN-II) and neurogenic muscle hypertrophy: a case report and literature review.

Authors: M Maurelli; E Candeloro; M T Egitto; E Alfonsi
Journal: Ital J Neurol Sci Date: 1998-06

2. NEFL E396K mutation is associated with a novel dominant intermediate Charcot-Marie-Tooth disease phenotype.

Authors: José Berciano; Antonio García; Kristien Peeters; Elena Gallardo; Els De Vriendt; Ana L Pelayo-Negro; Jon Infante; Albena Jordanova
Journal: J Neurol Date: 2015-04-01 Impact factor: 4.849

3. Comparison of CMT1A and CMT2: similarities and differences.

Authors: Henriette M E Bienfait; Camiel Verhamme; Ivo N van Schaik; Johannes H T M Koelman; Bram W Ongerboer de Visser; Rob J de Haan; Frank Baas; Baziel G M van Engelen; Marianne de Visser
Journal: J Neurol Date: 2006-08-28 Impact factor: 4.849

4. Somatosensory evoked potentials, sensory nerve potentials and sensory nerve conduction in hereditary motor and sensory neuropathy type I.

Authors: M Aramideh; J E Hoogendijk; C M Aalfs; F E Posthumus Meyjes; M De Visser; B W Ongerboer de Visser
Journal: J Neurol Date: 1992-05 Impact factor: 4.849

9. A combination of spastic paraparesis, polyneuropathy and adrenocortical insufficiency-a childhood form of adrenomyeloneuropathy.

Authors: K Toifl; B Mamoli; F Waldhauser
Journal: J Neurol Date: 1981 Impact factor: 4.849

10. Nerve conduction, tactile sensibility, and the electromyogram after suture or compression of peripheral nerve: a longitudinal study in man.

Authors: F Buchthal; V Kühl
Journal: J Neurol Neurosurg Psychiatry Date: 1979-05 Impact factor: 10.154

Peroneal muscular atrophy (PMA) and related disorders. I. Clinical manifestations as related to biopsy findings, nerve conduction and electromyography.

1. Hereditary motor and sensory neuropathy type II (HMSN-II) and neurogenic muscle hypertrophy: a case report and literature review.

2. NEFL E396K mutation is associated with a novel dominant intermediate Charcot-Marie-Tooth disease phenotype.

3. Comparison of CMT1A and CMT2: similarities and differences.

4. Somatosensory evoked potentials, sensory nerve potentials and sensory nerve conduction in hereditary motor and sensory neuropathy type I.

5. Hereditary motor and sensory neuropathy (HMSN) and optic atrophy (HMSN type VI, Vizioli).

6. Central motor conduction in a family with hereditary motor and sensory neuropathy with pyramidal signs (HMSN V).

Review 7. Diagnosis and treatment of chronic acquired demyelinating polyneuropathies.

8. Genetic linkage studies in hereditary motor and sensory neuropathies.

9. A combination of spastic paraparesis, polyneuropathy and adrenocortical insufficiency-a childhood form of adrenomyeloneuropathy.

10. Nerve conduction, tactile sensibility, and the electromyogram after suture or compression of peripheral nerve: a longitudinal study in man.