Neurodevelopmental and Cognitive Outcomes of Classical Homocystinuria: Experience from Qatar (Q35752496)

10 August 2017

Neurodevelopmental and Cognitive Outcomes of Classical Homocystinuria: Experience from Qatar (English)

1 reference

10 August 2017

1 reference

Haitham El Bashir

1

1 reference

10 August 2017

Lubna Dekair

series ordinal

2

1 reference

10 August 2017

Yasmeen Mahmoud

series ordinal

3

1 reference

10 August 2017

Tawfeg Ben-Omran

series ordinal

4

1 reference

10 August 2017

25 February 2015

1 reference

Journal of Inherited Metabolic Disorders Reports

10 August 2017

1 reference

10 August 2017

21

1 reference

10 August 2017

89-95

1 reference

Diagnostic and treatment implications of psychosis secondary to treatable metabolic disorders in adults: a systematic review

10 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4470953

Treatment of inherited homocystinurias.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4470953

A common mutation in the CBS gene explains a high incidence of homocystinuria in the Qatari population

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4470953

Socioeconomic status modifies heritability of IQ in young children

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4470953

HOMOCYSTINURIA: AN ENZYMATIC DEFECT.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4470953

The intellectual abilities of early-treated individuals with pyridoxine-nonresponsive homocystinuria due to cystathionine beta-synthase deficiency

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4470953

Heritability estimates versus large environmental effects: the IQ paradox resolved

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4470953

Cystathionine beta-synthase mutations in homocystinuria

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4470953

Newborn screening for homocystinuria: Irish and world experience

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4470953

2 October 2017

The heritability of IQ

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4470953

The natural history of homocystinuria due to cystathionine beta-synthase deficiency.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4470953

Psychiatric manifestations of homocystinuria due to cystathionine beta-synthase deficiency: prevalence, natural history, and relationship to neurologic impairment and vitamin B6-responsiveness

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4470953

Increased heritability for lower IQ levels?

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4470953

Paired comparisons between early treated PKU children and their matched sibling controls on intelligence and school achievement test results at eight years of age.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4470953

Vascular disease and homocysteine metabolism.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4470953

Neurologic and neurodevelopmental phenotypes in young children with early-treated combined methylmalonic acidemia and homocystinuria, cobalamin C type

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4470953

Newborn population screening for classic homocystinuria by determination of total homocysteine from Guthrie cards

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4470953

Saudi experience with classic homocystinuria.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4470953

Neurofibromatosis type 1 (Recklinghausen's disease). Neurologic and cognitive assessment with sibling controls.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4470953

Implementation of extended neonatal screening and a metabolic unit in the State of Qatar: developing and optimizing strategies in cooperation with the Neonatal Screening Center in Heidelberg

25 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25712383

12 December 2020

inferred from PubMed ID database lookup

Functional assays testing pathogenicity of 14 cystathionine-beta synthase mutations

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25712383

12 December 2020

inferred from PubMed ID database lookup

Molecular neonatal screening for homocystinuria in the Qatari population

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25712383

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/8904_2014_394

1 reference

release_5uko5tzyfbftlnps64vdbkpbu4

10 August 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/5uko5tzyfbftlnps64vdbkpbu4

24 November 2022

mapped directly with Wikidata item

PMCID

4470953

1 reference

10 August 2017

1 reference