Compounds > cysteine

cysteine and Adrenal Gland Hypofunction

cysteine has been researched along with Adrenal Gland Hypofunction in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (66.67)29.6817
2010's0 (0.00)24.3611
2020's1 (33.33)2.80

Authors

AuthorsStudies
Chugh, V; Dutt Sharma, S; Garg, M; Mangla, A; Mitharwal, P1
Deiss, D; Manns, MP; Strassburg, CP; Vogel, A1
Berger, J; Korosec, T; Molzer, B; Unterrainer, G1

Other Studies

3 other study(ies) available for cysteine and Adrenal Gland Hypofunction

ArticleYear
Non-classical lipoid adrenal hyperplasia presenting as hypoglycemic seizures.
    Journal of pediatric endocrinology & metabolism : JPEM, 2020, Nov-26, Volume: 33, Issue:11

    Topics: Adrenal Hyperplasia, Congenital; Adrenal Insufficiency; Amino Acid Substitution; Arginine; Child, Preschool; Cysteine; Diagnosis, Differential; Disorder of Sex Development, 46,XY; Female; Homozygote; Humans; Hypoglycemia; India; Mutation, Missense; Phosphoproteins; Seizures

2020
A novel AIRE mutation in an APECED patient with candidiasis, adrenal failure, hepatitis, diabetes mellitus and osteosclerosis.
    Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association, 2003, Volume: 111, Issue:3

    Topics: Adrenal Insufficiency; AIRE Protein; Amino Acid Substitution; Base Sequence; Cysteine; Diabetes Mellitus; Exons; Frameshift Mutation; Hepatitis; Heterozygote; History, 15th Century; Humans; Male; Osteosclerosis; Polyendocrinopathies, Autoimmune; Radiography; Threonine; Transcription Factors

2003
A de novo adrenoleukodystrophy gene (ABCD1) mutation S636I without detectable ABCD1 protein and a R104C mutation with normal amounts of protein from an Austrian patient collective.
    Human mutation, 2000, Volume: 16, Issue:6

    Topics: Adrenal Insufficiency; Adrenoleukodystrophy; Adult; Amino Acid Substitution; Arginine; ATP Binding Cassette Transporter, Subfamily D; ATP Binding Cassette Transporter, Subfamily D, Member 1; ATP-Binding Cassette Transporters; Cysteine; Humans; Isoleucine; Mutation, Missense; Proteins; Serine

2000