(Q48561662)

English

An infant with Marfanoid phenotype and congenital contractures associated with ocular and cardiovascular anomalies, cerebral white matter hypoplasia and spinal axonopathy.

scientific article published in January 1985

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scholarly article

1 reference

Europe PubMed Central

12 February 2018

http://europepmc.org/abstract/MED/3921377

An infant with Marfanoid phenotype and congenital contractures associated with ocular and cardiovascular anomalies, cerebral white matter hypoplasia and spinal axonopathy. (English)

1 reference

Europe PubMed Central

12 February 2018

http://europepmc.org/abstract/MED/3921377

author name string

P Tamminga

1

1 reference

Europe PubMed Central

12 February 2018

http://europepmc.org/abstract/MED/3921377

F G Jennekens

2

1 reference

Europe PubMed Central

12 February 2018

http://europepmc.org/abstract/MED/3921377

P G Barth

3

1 reference

Europe PubMed Central

12 February 2018

http://europepmc.org/abstract/MED/3921377

P Fleury

4

1 reference

Europe PubMed Central

12 February 2018

http://europepmc.org/abstract/MED/3921377

H van den Berg

5

1 reference

Europe PubMed Central

12 February 2018

http://europepmc.org/abstract/MED/3921377

J W Oorthuys

6

1 reference

Europe PubMed Central

12 February 2018

http://europepmc.org/abstract/MED/3921377

publication date

1 January 1985

1 reference

Europe PubMed Central

12 February 2018

http://europepmc.org/abstract/MED/3921377

European Journal of Pediatrics

1 reference

Europe PubMed Central

12 February 2018

http://europepmc.org/abstract/MED/3921377

143

1 reference

Europe PubMed Central

12 February 2018

http://europepmc.org/abstract/MED/3921377

3

1 reference

Europe PubMed Central

12 February 2018

http://europepmc.org/abstract/MED/3921377

228-231

1 reference

Europe PubMed Central

12 February 2018

http://europepmc.org/abstract/MED/3921377

https://scigraph.springernature.com/pub.10.1007/bf00442148

0 references

Early cardiac manifestations of Marfan's syndrome in the newborn

1 reference

https://pubmed.ncbi.nlm.nih.gov/3921377

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenitale kontrakturelle Arachnodaktylie (CCA-Syndrom) - Eine autosomal dominant erbliche Bindegewebserkrankung

1 reference

https://pubmed.ncbi.nlm.nih.gov/3921377

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital contractural arachnodactyly and intraocular colobomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/3921377

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multisystem neuronal degeneration, hepatosplenomegaly, and adrenocortical deficiency associated with reduced tissue arachidonic acid

1 reference

https://pubmed.ncbi.nlm.nih.gov/3921377

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The distal arthrogryposes: delineation of new entities--review and nosologic discussion

1 reference

https://pubmed.ncbi.nlm.nih.gov/3921377

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Marfan syndrome with contractural arachnodactyly and severe mitral regurgitation in a premature infant

1 reference

https://pubmed.ncbi.nlm.nih.gov/3921377

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

"New" syndrome of congenital contractural arachnodactyly originally described by Marfan in 1896

1 reference

https://pubmed.ncbi.nlm.nih.gov/3921377

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cerebral white-matter hypoplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/3921377

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypoplasia of hemispheric white matter, peculiar pallidal changes and dysplastic inferior olives in a child with psychomotor retardation

1 reference

https://pubmed.ncbi.nlm.nih.gov/3921377

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Infantile neuroaxonal dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/3921377

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical variability in the Marfan syndrome(s)

1 reference

https://pubmed.ncbi.nlm.nih.gov/3921377

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00442148

1 reference

Europe PubMed Central

12 February 2018

http://europepmc.org/abstract/MED/3921377

1 reference

Europe PubMed Central

12 February 2018

http://europepmc.org/abstract/MED/3921377

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