tryptophan and Adrenal Hyperplasia, Congenital

tryptophan has been researched along with Adrenal Hyperplasia, Congenital in 3 studies

Research

Studies (3)

Timeframe	Studies, this research(%)	All Research%
pre-1990	1 (33.33)	18.7374
1990's	1 (33.33)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (33.33)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Choi, JH; Kang, M; Kim, GH; Kim, SY; Kim, YM; Lee, BH; Ohn, JH; Park, MS; Yoo, HW	1
Chiou, SH; Chung, BC; Hu, MC	1
Tabolin, VA	1

Reviews

1 review(s) available for tryptophan and Adrenal Hyperplasia, Congenital

Article	Year
A review of the literature on common CYP17A1 mutations in adults with 17-hydroxylase/17,20-lyase deficiency, a case series of such mutations among Koreans and functional characteristics of a novel mutation. Metabolism: clinical and experimental, 2014, Volume: 63, Issue:1 Topics: Adolescent; Adrenal Hyperplasia, Congenital; Adult; Asian People; DNA Mutational Analysis; Founder Effect; Gene Frequency; Glucocorticoids; Heterozygote; Histidine; Humans; Hypertension; Leucine; Models, Chemical; Mutation; Polymerase Chain Reaction; Prednisolone; Republic of Korea; Steroid 17-alpha-Hydroxylase; Tryptophan	2014

Article

Year

A review of the literature on common CYP17A1 mutations in adults with 17-hydroxylase/17,20-lyase deficiency, a case series of such mutations among Koreans and functional characteristics of a novel mutation.

Metabolism: clinical and experimental, 2014, Volume: 63, Issue:1

Topics: Adolescent; Adrenal Hyperplasia, Congenital; Adult; Asian People; DNA Mutational Analysis; Founder Effect; Gene Frequency; Glucocorticoids; Heterozygote; Histidine; Humans; Hypertension; Leucine; Models, Chemical; Mutation; Polymerase Chain Reaction; Prednisolone; Republic of Korea; Steroid 17-alpha-Hydroxylase; Tryptophan

2014

Other Studies

2 other study(ies) available for tryptophan and Adrenal Hyperplasia, Congenital

Article	Year
A missense mutation at Ile172----Asn or Arg356----Trp causes steroid 21-hydroxylase deficiency. The Journal of biological chemistry, 1990, Feb-25, Volume: 265, Issue:6 Topics: Adolescent; Adrenal Hyperplasia, Congenital; Arginine; Asparagine; Base Sequence; Codon; DNA; Female; Genes; Humans; Isoleucine; Molecular Sequence Data; Mutation; Oligonucleotide Probes; Plasmids; Reference Values; Restriction Mapping; Steroid 21-Hydroxylase; Steroid Hydroxylases; Transfection; Tryptophan	1990
[Metabolic disorders, their early diagnosis and therapy in newborn infants]. Vestnik Akademii meditsinskikh nauk SSSR, 1973, Volume: 28, Issue:6 Topics: Adrenal Hyperplasia, Congenital; Amino Acid Metabolism, Inborn Errors; Carbohydrate Metabolism, Inborn Errors; Child, Preschool; Cystic Fibrosis; Fanconi Syndrome; Humans; Hyperbilirubinemia, Hereditary; Immunologic Deficiency Syndromes; Infant; Infant, Newborn; Jaundice, Neonatal; Malabsorption Syndromes; Neurologic Manifestations; Phenylketonurias; Tryptophan	1973

Article

Year

A missense mutation at Ile172----Asn or Arg356----Trp causes steroid 21-hydroxylase deficiency.

The Journal of biological chemistry, 1990, Feb-25, Volume: 265, Issue:6

Topics: Adolescent; Adrenal Hyperplasia, Congenital; Arginine; Asparagine; Base Sequence; Codon; DNA; Female; Genes; Humans; Isoleucine; Molecular Sequence Data; Mutation; Oligonucleotide Probes; Plasmids; Reference Values; Restriction Mapping; Steroid 21-Hydroxylase; Steroid Hydroxylases; Transfection; Tryptophan

1990

[Metabolic disorders, their early diagnosis and therapy in newborn infants].

Vestnik Akademii meditsinskikh nauk SSSR, 1973, Volume: 28, Issue:6

Topics: Adrenal Hyperplasia, Congenital; Amino Acid Metabolism, Inborn Errors; Carbohydrate Metabolism, Inborn Errors; Child, Preschool; Cystic Fibrosis; Fanconi Syndrome; Humans; Hyperbilirubinemia, Hereditary; Immunologic Deficiency Syndromes; Infant; Infant, Newborn; Jaundice, Neonatal; Malabsorption Syndromes; Neurologic Manifestations; Phenylketonurias; Tryptophan

1973