Prevalence of congenital adrenal hyperplasia among sudden infant death in the Czech Republic and Austria (Q58025156)

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scholarly article by Kristina A. Strnadová et al published 22 September 2006 in European Journal of Pediatrics

Language	Label	Description	Also known as
English	Prevalence of congenital adrenal hyperplasia among sudden infant death in the Czech Republic and Austria	scholarly article by Kristina A. Strnadová et al published 22 September 2006 in European Journal of Pediatrics

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scholarly article

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Prevalence of congenital adrenal hyperplasia among sudden infant death in the Czech Republic and Austria (English)

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congenital adrenal hyperplasia

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object named as

Jan Lebl

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author name string

Kristina A. Strnadová

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Felix Votava

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Adolf Mühl

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Chike Item

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Olaf A. Bodamer

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Toni Torresani

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Ivan Bouška

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Franz Waldhauser

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Wolfgang Sperl

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language of work or name

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publication date

22 September 2006

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European Journal of Pediatrics

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166

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1

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1-4

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https://scigraph.springernature.com/pub.10.1007/s00431-006-0154-8

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Phenotype and genotype correlation of the microconversion from the CYP21A1P to the CYP21A2 gene in congenital adrenal hyperplasia.

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https://api.crossref.org/works/10.1007%2FS00431-006-0154-8

21 January 2018

Stability of 17alpha-hydroxyprogesterone in dried blood spots after autoclaving and prolonged storage.

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https://pubmed.ncbi.nlm.nih.gov/17024350

12 December 2020

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Genotyping of CYP21, linked chromosome 6p markers, and a sex-specific gene in neonatal screening for congenital adrenal hyperplasia

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https://pubmed.ncbi.nlm.nih.gov/17024350

12 December 2020

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Congenital adrenal hyperplasia: phenotype and genotype.

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https://pubmed.ncbi.nlm.nih.gov/17024350

12 December 2020

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Screening for congenital adrenal hyperplasia: adjustment of 17-hydroxyprogesterone cut-off values to both age and birth weight markedly improves the predictive value

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https://pubmed.ncbi.nlm.nih.gov/17024350

12 December 2020

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Results of screening 1.9 million Texas newborns for 21-hydroxylase-deficient congenital adrenal hyperplasia.

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https://pubmed.ncbi.nlm.nih.gov/17024350

12 December 2020

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Evaluation of neonatal screening for congenital adrenal hyperplasia

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https://pubmed.ncbi.nlm.nih.gov/17024350

12 December 2020

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Sudden infant death syndrome and unclassified sudden infant deaths: a definitional and diagnostic approach

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https://pubmed.ncbi.nlm.nih.gov/17024350

12 December 2020

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Lessons from 30 years of clinical diagnosis and treatment of congenital adrenal hyperplasia in five middle European countries

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https://pubmed.ncbi.nlm.nih.gov/17024350

12 December 2020

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Congenital adrenal hyperplasia due to 21-hydroxylase deficiency

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https://pubmed.ncbi.nlm.nih.gov/17024350

12 December 2020

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Cardiac arrest in an infant with congenital adrenal hyperplasia

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https://pubmed.ncbi.nlm.nih.gov/17024350

12 December 2020

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Worldwide experience in newborn screening for classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency

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https://pubmed.ncbi.nlm.nih.gov/17024350

12 December 2020

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Neonatal screening program for congenital adrenal hyperplasia: adjustments to the recall protocol

1 reference

https://pubmed.ncbi.nlm.nih.gov/17024350

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00431-006-0154-8

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