(Q48555626)

12 February 2018

title

Is Werdnig-Hoffmann disease a pure lower motor neuron disorder? (English)

1 reference

12 February 2018

main subject

Werdnig–Hoffmann disease

1 reference

J Towfighi

1

1 reference

12 February 2018

R S Young

series ordinal

2

1 reference

12 February 2018

R M Ward

series ordinal

3

1 reference

12 February 2018

publication date

1 January 1985

1 reference

12 February 2018

published in

Acta Neuropathologica

1 reference

12 February 2018

volume

65

1 reference

12 February 2018

issue

3-4

1 reference

12 February 2018

page(s)

270-280

1 reference

12 February 2018

https://scigraph.springernature.com/pub.10.1007/bf00687008

exact match

0 references

cites work

Anoxic-ischemic encephalopathy in the human neonatal period. The significance of brain stem involvement

1 reference

12 December 2020

Regular involvement of Clarke's nucleus in sporadic amyotrophic lateral sclerosis.

1 reference

12 December 2020

Sensory system involvement in infantile spinal muscular atrophy

1 reference

12 December 2020

[Supraspinobulbar lesions in Wernig-Hoffman amyotrophy]

1 reference

12 December 2020

Cerebellar hypoplasia in Werdnig-Hoffmann disease

1 reference

12 December 2020

[Thalamic lesions in myotonia in infant]

1 reference

12 December 2020

CEREBELLO-THALAMO-SPINAL DEGENERATION IN INFANCY: AN UNUSUAL VARIANT OF WERDNIG-HOFFMANN DISEASE.

1 reference

12 December 2020

Juvenile spinal muscular atrophy: a new hexosaminidase deficiency phenotype

1 reference

12 December 2020

Sensory ganglioneuropathy in infantile spinal muscular atrophy. Light and electronmicroscopic findings in two cases

1 reference

12 December 2020

Peripheral Motor and Sensory Neuropathy of Early Childhood, Simulating Werdnig-Hoffmann Disease

1 reference

12 December 2020

Infantile muscular atrophy

1 reference

12 December 2020

[Werdnig-Hoffmann's infantile progressive muscular atrophy; clinical aspects, pathology, heredity, and relation to Oppenheim's amyotonia congenita and other morbid conditions with laxity of the joints or muscles in children.]

1 reference

12 December 2020

Normal vitamin E status in spinal muscular atrophy

1 reference

12 December 2020

[Cerebellar hypogenesis in a family with Werdnig-Hoffmann's amyotrophy; histopathological bases]

1 reference

12 December 2020

Pathological Findings in Werdnig-Hoffmann’s Disease with Special Remarks on Diencephalic Lesions

1 reference

12 December 2020

Progressive neuropathologic lesions in vitamin E-deficient rhesus monkeys

1 reference

12 December 2020

Frequency of nerve fiber degeneration of peripheral motor and sensory neurons in amyotrophic lateral sclerosis. Morphometry of deep and superficial peroneal nerves

1 reference

12 December 2020

Infantile neuronal degeneration masquerading as Werdnig-Hoffmann disease

1 reference

12 December 2020

The nosology of the spinal muscular atrophies

1 reference

12 December 2020

Effects of chronic vitamin E deficiency on the nervous system of the rat

1 reference

12 December 2020

Cerebellar Hypoplasia in Werdnig-Hoffmann Disease

1 reference

12 December 2020

Anterior horn cell disease associated with pontocerebellar hypoplasia in infants

1 reference

12 December 2020

Axonal dystrophy in the gracile nucleus in congenital biliary atresia and cystic fibrosis (mucoviscidosis): beneficial effect of vitamin E therapy

1 reference

12 December 2020

Familial amyotrophic lateral sclerosis. A subgroup characterized by posterior and spinocerebellar tract involvement and hyaline inclusions in the anterior horn cells

1 reference

12 December 2020

Pathological involvement of primary sensory neurons in Werdnig-Hoffmann disease

1 reference

12 December 2020

Werdnig-Hoffmann disease: Proposal of a pathogenetic mechanism

1 reference

12 December 2020

[Spinal amyotrophia in children (Werdnig-Hoffmann paralysis) as hereditary degeneration.]

1 reference

12 December 2020

Morphological and morphometric studies on the spinal cord lesion in Werdnig-Hoffmann disease.

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00687008

1 reference

12 February 2018

1 reference

12 February 2018