(Q36921664)

English

Effect of the parental origin of the X-chromosome on the clinical features, associated complications, the two-year-response to growth hormone (rhGH) and the biochemical profile in patients with turner syndrome.

scientific article published on 04 June 2013

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23731950%20AND%20SRC:MED&resulttype=core&format=json

2 March 2020

Effect of the parental origin of the X-chromosome on the clinical features, associated complications, the two-year-response to growth hormone (rhGH) and the biochemical profile in patients with turner syndrome (English)

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23731950%20AND%20SRC:MED&resulttype=core&format=json

2 March 2020

biochemical profile

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based on heuristic

inferred from title

2

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2 March 2020

Verónica Mericq

6

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2 March 2020

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Francisco Alvarez-Nava

1

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2 March 2020

José Miguel Quintero

3

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2 March 2020

Mirta Miras

4

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2 March 2020

Hugo Fideleff

5

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2 March 2020

Henry Marcano

7

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2 March 2020

William Zabala

8

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2 March 2020

Marisol Soto

9

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2 March 2020

Tatiana Pardo

10

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2 March 2020

Lisbeth Borjas

11

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2 March 2020

Joalice Villalobos

12

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2 March 2020

Peter Gunczler

13

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2 March 2020

Nancy Unanue

14

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2 March 2020

Natalia Tkalenko

15

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2 March 2020

Adriana Boyanofsky

16

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Europe PubMed Central

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2 March 2020

Liliana Silvano

17

1 reference

Europe PubMed Central

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2 March 2020

Liliana Franchioni

18

1 reference

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2 March 2020

Miriam Llano

19

1 reference

Europe PubMed Central

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2 March 2020

Gabriel Fideleff

20

1 reference

Europe PubMed Central

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2 March 2020

Miriam Azaretzky

21

1 reference

Europe PubMed Central

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2 March 2020

Martha Suarez

22

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2 March 2020

publication date

4 June 2013

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2 March 2020

International journal of pediatric endocrinology

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23731950%20AND%20SRC:MED&resulttype=core&format=json

2 March 2020

2013

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2 March 2020

1

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Europe PubMed Central

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2 March 2020

10

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23731950%20AND%20SRC:MED&resulttype=core&format=json

2 March 2020

Genomic imprinting and Turner syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679778

29 September 2017

A GEP-ISFG collaborative study on the optimization of an X-STR decaplex: data on 15 Iberian and Latin American populations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679778

29 September 2017

Epidemiological, endocrine and metabolic features in Turner syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679778

29 September 2017

Molecular analysis in Turner syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679778

29 September 2017

Parental origin of normal X chromosomes in Turner syndrome patients with various karyotypes: implications for the mechanism leading to generation of a 45,X karyotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679778

29 September 2017

Microsatellite analysis in Turner syndrome: Parental origin of X chromosomes and possible mechanism of formation of abnormal chromosomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679778

29 September 2017

Parental origin-dependent, male offspring-specific transmission-ratio distortion at loci on the human X chromosome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679778

29 September 2017

Possible role of imprinting in the Turner phenotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679778

29 September 2017

The distribution of chromosomal genotypes associated with Turner's syndrome: livebirth prevalence rates and evidence for diminished fetal mortality and severity in genotypes associated with structural X abnormalities or mosaicism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679778

29 September 2017

Growth curve for girls with Turner syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679778

29 September 2017

Cytogenetic and molecular analysis of sex-chromosome monosomy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679778

29 September 2017

Analysis of the origin of Turner's syndrome using polymorphic DNA probes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679778

29 September 2017

The parental origin of the single X chromosome in Turner syndrome: lack of correlation with parental age or clinical phenotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679778

29 September 2017

GHR and VDR Genes do not Contribute to the Growth Hormone (GH) Response in GH Deficient and Turner Syndrome Patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679778

27 June 2018

The physical phenotype of girls and women with Turner syndrome is not X-imprinted.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679778

27 June 2018

Molecular studies of parental origin and mosaicism in 45,X conceptuses

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679778

27 June 2018

Parental origin of the X-chromosome does not influence growth hormone treatment effect in Turner syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679778

4 September 2018

Influence of parental origin of the X chromosome on physical phenotypes and GH responsiveness of patients with Turner syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679778

4 September 2018

The influence of parental origin of X chromosome genes on the stature of patients with 45 X Turner syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679778

4 September 2018

Clinical significance of the parental origin of the X chromosome in turner syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679778

4 September 2018

Genomic imprinting in Turner syndrome: effects on response to growth hormone and on risk of sensorineural hearing loss

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679778

4 September 2018

Increased prevalence of ADHD in Turner syndrome with no evidence of imprinting effects.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679778

4 September 2018

Sequence variation and allele nomenclature for the X-linked STRs DXS9895, DXS8378, DXS7132, DXS6800, DXS7133, GATA172D05, DXS7423 and DXS8377.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679778

4 September 2018

Lipid abnormalities in Turner syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3679778

4 September 2018

Body composition is distinctly altered in Turner syndrome: relations to glucose metabolism, circulating adipokines, and endothelial adhesion molecules

1 reference

https://api.crossref.org/works/10.1186%2F1687-9856-2013-10

21 January 2018

Maternal X Chromosome, Visceral Adiposity, and Lipid Profile

1 reference

https://api.crossref.org/works/10.1186%2F1687-9856-2013-10

21 January 2018

Growth retardation in Turner syndrome: aneuploidy, rather than specific gene loss, may explain growth failure

1 reference

https://pubmed.ncbi.nlm.nih.gov/23731950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular genetics of Turner syndrome: correlation with clinical phenotype and response to growth hormone therapy

1 reference

https://pubmed.ncbi.nlm.nih.gov/23731950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular study of 45,X conceptuses: correlation with clinical findings

1 reference

https://pubmed.ncbi.nlm.nih.gov/23731950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Serum lipids, lipoprotein lp(a), and plasminogen activator inhibitor-1 in patients with Turner's syndrome before and during growth hormone and estrogen therapy

1 reference

https://pubmed.ncbi.nlm.nih.gov/23731950

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/1687-9856-2013-10

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23731950%20AND%20SRC:MED&resulttype=core&format=json

2 March 2020

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2 March 2020

PubMed publication ID

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Europe PubMed Central

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2 March 2020

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