(Q41357948)

29 September 2017

Congenital hypomyelinating neuropathy: a reversible case (English)

1 reference

29 September 2017

0 references

Ghamdi M

1

1 reference

29 September 2017

Armstrong DL

series ordinal

2

1 reference

29 September 2017

Miller G

series ordinal

3

1 reference

29 September 2017

1 January 1997

1 reference

29 September 2017

1 reference

29 September 2017

16

1 reference

29 September 2017

1

1 reference

29 September 2017

71-73

1 reference

Heterogeneity of congenital motor and sensory neuropathies

29 September 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900262-7

7 January 2021

Muscle and intramuscular nerve pathology in congenital hypomyelination neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900262-7

7 January 2021

Morphometric studies of normal sural nerves in children.

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900262-7

7 January 2021

Congenital absence of peripheral myelin: abnormal Schwann cell development causes lethal arthrogryposis multiplex congenita

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900262-7

7 January 2021

Hypomyelination neuropathy in a female newborn presenting as arthrogryposis multiplex congenita.

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900262-7

7 January 2021

Chronic polyradiculoneuropathy of infancy. A report of three cases with familial incidence

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900262-7

7 January 2021

Hypertrophic interstitial polyneuropathy in infancy. Clinical and pathologic features in two cases.

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900262-7

7 January 2021

Connatal polyneuropathy ? A case with proliferated microfilaments in schwann cells

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900262-7

7 January 2021

Infantile Hereditary Neuropathy with Hypomyelination: Report of Two Siblings with Different Expressivity

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900262-7

7 January 2021

Charcot-Marie-Tooth disease: a new paradigm for the mechanism of inherited disease

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900262-7

7 January 2021

Connexin mutations in X-linked Charcot-Marie-Tooth disease

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900262-7

7 January 2021

Deletion of the serine 34 codon from the major peripheral myelin protein P0 gene in Charcot-Marie-Tooth disease type 1B

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900262-7

7 January 2021

De novo mutation of the myelin P0 gene in Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III)

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900262-7

7 January 2021

Dejerine-Sottas syndrome associated with point mutation in the peripheral myelin protein 22 (PMP22) gene

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900262-7

7 January 2021

Benign infantile mitochondrial myopathy due to reversible cytochrome c oxidase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2896%2900262-7

7 January 2021

10.1016/S0887-8994(96)00262-7

Identifiers

DOI

1 reference

release_bpioalwazzf4hex6bzhmi464y4

29 September 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/bpioalwazzf4hex6bzhmi464y4

24 November 2022

mapped directly with Wikidata item

1 reference