(Q41938132)

English

Pontocerebellar hypoplasia type III (CLAM): extended phenotype and novel molecular findings

scientific article published on 14 March 2009

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

Pontocerebellar hypoplasia type III (CLAM): extended phenotype and novel molecular findings (English)

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

2

object named as

Bernd Wollnik

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

author name string

Burak Durmaz

1

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

Ozgur Cogulu

3

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

Yun Li

4

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

Hasan Tekgul

5

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

Filiz Hazan

6

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

Ferda Ozkinay

7

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

publication date

14 March 2009

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

Journal of Neurology

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

256

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

416-419

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

A novel form of pontocerebellar hypoplasia maps to chromosome 7q11-21.

1 reference

https://api.crossref.org/works/10.1007%2FS00415-009-0094-0

21 January 2018

A syndrome of autosomal recessive pontocerebellar hypoplasia with white matter abnormalities and protracted course in two brothers.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19277761

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MR findings in pontocerebellar hypoplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/19277761

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital pontocerebellar atrophy in three patients: clinical, radiologic and etiologic considerations.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19277761

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Infantile olivopontocerebellar atrophy with spinal muscular atrophy (infantile OPCA + SMA).

1 reference

https://pubmed.ncbi.nlm.nih.gov/19277761

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pontocerebellar hypoplasias. An overview of a group of inherited neurodegenerative disorders with fetal onset

1 reference

https://pubmed.ncbi.nlm.nih.gov/19277761

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pontocerebellar hypoplasia type 2 (PCH2): report of two siblings

1 reference

https://pubmed.ncbi.nlm.nih.gov/19277761

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Extended phenotype of pontocerebellar hypoplasia with infantile spinal muscular atrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/19277761

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fourteen novel human members of mitochondrial solute carrier family 25 (SLC25) widely expressed in the central nervous system.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19277761

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomics of the human carnitine acyltransferase genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/19277761

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pontocerebellar hypoplasia in two siblings with dysmorphic features

1 reference

https://pubmed.ncbi.nlm.nih.gov/19277761

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00415-009-0094-0

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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