(Q41925675)

English

Developmental patterns and neuropsychological assessment in patients with carbohydrate-deficient glycoconjugate syndrome type IA (phosphomannomutase deficiency).

scientific article published on June 1999

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

Developmental patterns and neuropsychological assessment in patients with carbohydrate-deficient glycoconjugate syndrome type IA (phosphomannomutase deficiency). (English)

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

neuropsychology

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based on heuristic

inferred from title

1

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Europe PubMed Central

PubMed publication ID

14 October 2017

author name string

Pavone L

2

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

Fiumara A

3

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

Bianchini R

4

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

Jaeken J

5

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Europe PubMed Central

PubMed publication ID

14 October 2017

publication date

1 June 1999

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Europe PubMed Central

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14 October 2017

Brain and Development

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Europe PubMed Central

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14 October 2017

21

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Europe PubMed Central

PubMed publication ID

14 October 2017

4

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Europe PubMed Central

PubMed publication ID

14 October 2017

260-263

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Europe PubMed Central

PubMed publication ID

14 October 2017

Carbohydrate-deficient glycoconjugate (CDG) syndromes: a new chapter of neuropaediatrics

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2899%2900020-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations in PMM2, a phosphomannomutase gene on chromosome 16p13, in carbohydrate-deficient glycoprotein type I syndrome (Jaeken syndrome)

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2899%2900020-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Carbohydrate deficient glycoprotein (CDG) syndrome type I

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2899%2900020-0

7 January 2021

based on heuristic

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Olivopontocerebellar atrophy leading to recognition of carbohydrate-deficient glycoprotein syndrome type I.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2899%2900020-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Carbohydrate-deficient glycoprotein syndrome: clinical expression in adults with a new metabolic disease

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2899%2900020-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Autosomal recessive congenital cerebellar atrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2899%2900020-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Cognitive deficits in olivopontocerebellar atrophy: implications for the cholinergic hypothesis of Alzheimer's dementia

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2899%2900020-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Reappraising the cerebellum: what does the hindbrain contribute to the forebrain?

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2899%2900020-0

7 January 2021

based on heuristic

inferred from DOI database lookup

The cerebellum and cognitive functions in humans.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2899%2900020-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0387-7604(99)00020-0

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

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