(Q44762047)

English

Ehlers-Danlos syndrome type VI with cystic malformations of the meninges in a 7-year-old girl

scientific article published on 11 February 2004

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

Ehlers-Danlos syndrome type VI with cystic malformations of the meninges in a 7-year-old girl (English)

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

Ehlers-Danlos syndrome

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author name string

Irene Brunk

1

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

Brigitte Stöver

2

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

Chrysanthy Ikonomidou

3

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

Jürgen Brinckmann

4

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

Luitgard M Neumann

5

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

language of work or name

1 reference

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publication date

11 February 2004

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Europe PubMed Central

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6 December 2017

European Journal of Pediatrics

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Europe PubMed Central

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6 December 2017

163

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6 December 2017

4-5

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Europe PubMed Central

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6 December 2017

214-217

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6 December 2017

Ehlers-Danlos syndrome type VI: Cross-link pattern in tissue and urine sample as a diagnostic marker

1 reference

https://pubmed.ncbi.nlm.nih.gov/14872341

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the lysyl hydroxylase 1 gene that result in enzyme deficiency and the clinical phenotype of Ehlers-Danlos syndrome type VI.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14872341

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Different pattern of collagen cross-links in two sclerotic skin diseases: lipodermatosclerosis and circumscribed scleroderma.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14872341

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple meningeal cysts in Marfan syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/14872341

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Urinary pyridinium cross-links: a noninvasive diagnostic test for Ehlers-Danlos syndrome type VI

1 reference

https://pubmed.ncbi.nlm.nih.gov/14872341

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[A case of sacral meningeal cyst with Marfan syndrome]

1 reference

https://pubmed.ncbi.nlm.nih.gov/14872341

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ehlers-Danlos Syndrome Type VI (EDS VI): problems of diagnosis and management

1 reference

https://pubmed.ncbi.nlm.nih.gov/14872341

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biochemical characterization of variants of the Ehlers-Danlos syndrome type VI

1 reference

https://pubmed.ncbi.nlm.nih.gov/14872341

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lysyl-protocollagen hydroxylase deficiency in fibroblasts from siblings with hydroxylysine-deficient collagen

1 reference

https://pubmed.ncbi.nlm.nih.gov/14872341

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Urinary pyridinoline cross-links in Ehlers-Danlos syndrome type VI.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14872341

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hydroxylysine-deficient skin collagen in a patient with a form of the Ehlers-Danlos syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14872341

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ehlers-Danlos syndromes: revised nosology, Villefranche, 1997. Ehlers-Danlos National Foundation (USA) and Ehlers-Danlos Support Group (UK).

1 reference

https://pubmed.ncbi.nlm.nih.gov/14872341

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ehlers-Danlos syndrome type VI: clinical manifestations of collagen lysyl hydroxylase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/14872341

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Heritable Disorder of Connective Tissue

1 reference

https://pubmed.ncbi.nlm.nih.gov/14872341

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ehlers-Danlos syndrome associated with multiple spinal meningeal cysts--case report

1 reference

https://pubmed.ncbi.nlm.nih.gov/14872341

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sacral Abnormalities in Marfan Syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/14872341

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00431-004-1407-Z

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

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