(Q28185471)

English

Biotinidase deficiency: clinical and MRI findings consistent with myelopathy

scientific article (publication date: July 2003)

In more languages

edit

Statements

instance of

scholarly article

0 references

title

Biotinidase deficiency: clinical and MRI findings consistent with myelopathy (English)

0 references

main subject

biotinidase deficiency

1 reference

Max Wiznitzer

1

0 references

Barbara A Bangert

series ordinal

2

0 references

language of work or name

English

0 references

publication date

July 2003

0 references

published in

Pediatric Neurology

0 references

volume

29

0 references

issue

1

0 references

page(s)

56-8

0 references

cites work

Phenotypic variation in biotinidase deficiency

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0887-8994%2803%2900042-0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Biotinidase deficiency: initial clinical features and rapid diagnosis.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0887-8994%2803%2900042-0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Biotinidase deficiency: a survey of 10 cases

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0887-8994%2803%2900042-0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

A biotinidase Km variant causing late onset bilateral optic neuropathy

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0887-8994%2803%2900042-0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Late presentation of biotinidase deficiency with acute visual loss and gait disturbance.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0887-8994%2803%2900042-0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Biotinidase deficiency with neurological features resembling multiple sclerosis

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0887-8994%2803%2900042-0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Delayed-onset profound biotinidase deficiency

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0887-8994%2803%2900042-0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Biotinidase deficiency: a cause of subacute necrotizing encephalomyelopathy (Leigh syndrome). Report of a case with lethal outcome

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0887-8994%2803%2900042-0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Neuropathology of biotinidase deficiency

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0887-8994%2803%2900042-0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Intermittent ataxia and immunodeficiency with multiple carboxylase deficiencies: a biotin-responsive disorder

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0887-8994%2803%2900042-0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

DOI

10.1016/S0887-8994(03)00042-0

0 references

PubMed publication ID

13679123

0 references

(Q28185471)

Biotinidase deficiency: clinical and MRI findings consistent with myelopathy

Statements

Identifiers

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)