Page last updated: 2024-08-17

histidine and Diaphragmatic Hernia

histidine has been researched along with Diaphragmatic Hernia in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (50.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Antonius, T; Eggink, A; Noordam, K; van Bon, B; van der Burgt, I; van Heijst, A	1
de Zegher, F; Deloof, E; Devlieger, H; Devriendt, K; Legius, E; Moerman, P; Proesmans, W; Vanhole, C	1

Other Studies

2 other study(ies) available for histidine and Diaphragmatic Hernia

Article	Year
Denys-Drash syndrome and congenital diaphragmatic hernia: another case with the 1097G > A(Arg366His) mutation. American journal of medical genetics. Part A, 2008, Feb-15, Volume: 146A, Issue:4 Topics: Arginine; Denys-Drash Syndrome; Fatal Outcome; Female; Genes, Wilms Tumor; Hernia, Diaphragmatic; Hernias, Diaphragmatic, Congenital; Histidine; Humans; Infant, Newborn; Male; Point Mutation	2008
Diaphragmatic hernia in Denys-Drash syndrome. American journal of medical genetics, 1995, May-22, Volume: 57, Issue:1 Topics: Animals; Arginine; Base Sequence; Chromosomes, Human, Pair 11; Disorders of Sex Development; DNA-Binding Proteins; Exons; Female; Gene Deletion; Genes, Tumor Suppressor; Gonadal Dysgenesis; Hernia, Diaphragmatic; Heterozygote; Histidine; Homozygote; Humans; Infant, Newborn; Kidney Glomerulus; Mice; Mice, Transgenic; Molecular Sequence Data; Ovary; Point Mutation; Syndrome; Transcription Factors; WT1 Proteins	1995

Article

Year

Denys-Drash syndrome and congenital diaphragmatic hernia: another case with the 1097G > A(Arg366His) mutation.

American journal of medical genetics. Part A, 2008, Feb-15, Volume: 146A, Issue:4

Topics: Arginine; Denys-Drash Syndrome; Fatal Outcome; Female; Genes, Wilms Tumor; Hernia, Diaphragmatic; Hernias, Diaphragmatic, Congenital; Histidine; Humans; Infant, Newborn; Male; Point Mutation

2008

Diaphragmatic hernia in Denys-Drash syndrome.

American journal of medical genetics, 1995, May-22, Volume: 57, Issue:1

Topics: Animals; Arginine; Base Sequence; Chromosomes, Human, Pair 11; Disorders of Sex Development; DNA-Binding Proteins; Exons; Female; Gene Deletion; Genes, Tumor Suppressor; Gonadal Dysgenesis; Hernia, Diaphragmatic; Heterozygote; Histidine; Homozygote; Humans; Infant, Newborn; Kidney Glomerulus; Mice; Mice, Transgenic; Molecular Sequence Data; Ovary; Point Mutation; Syndrome; Transcription Factors; WT1 Proteins

1995