tryptophan and Addison Disease

tryptophan has been researched along with Addison Disease in 4 studies

Research

Studies (4)

Timeframe	Studies, this research(%)	All Research%
pre-1990	1 (25.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	3 (75.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Cordell, H; Donaldson, P; Fichna, M; Fichna, P; Gryczyńska, M; Januszkiewicz-Lewandowska, D; McDonald, D; Nowak, J; Owen, K; Pearce, S; Roycroft, M; Zurawek, M	1
Braun, R; Handschug, K; Huebner, A; Kaindl, AM	1
Ball, SG; Donaldson, PT; Herington, S; James, RA; Jennings, CE; Owen, CJ; Pearce, SH; Perros, P; Quinton, R; Velaga, MR; Wilson, V	1
Leonard, BE	1

Reviews

2 review(s) available for tryptophan and Addison Disease

Article	Year
The tryptophan 620 allele of the lymphoid tyrosine phosphatase (PTPN22) gene predisposes to autoimmune Addison's disease. Clinical endocrinology, 2009, Volume: 70, Issue:3 Topics: Addison Disease; Autoimmune Diseases; Case-Control Studies; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Poland; Polymorphism, Single Nucleotide; Protein Tyrosine Phosphatase, Non-Receptor Type 22; Tryptophan; United Kingdom; White People	2009
Neurochemical and neuropharmacological aspects of depression. International review of neurobiology, 1975, Volume: 18 Topics: Addison Disease; Adrenal Cortex Hormones; Amphetamines; Animals; Antidepressive Agents, Tricyclic; Bipolar Disorder; Brain; Cushing Syndrome; Cyclic AMP; Depression; Electroconvulsive Therapy; Humans; Lithium; Methyltyrosines; Monoamine Oxidase Inhibitors; Neurotransmitter Agents; Reserpine; Tryptophan	1975

Article

Year

The tryptophan 620 allele of the lymphoid tyrosine phosphatase (PTPN22) gene predisposes to autoimmune Addison's disease.

Clinical endocrinology, 2009, Volume: 70, Issue:3

Topics: Addison Disease; Autoimmune Diseases; Case-Control Studies; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Poland; Polymorphism, Single Nucleotide; Protein Tyrosine Phosphatase, Non-Receptor Type 22; Tryptophan; United Kingdom; White People

2009

Neurochemical and neuropharmacological aspects of depression.

International review of neurobiology, 1975, Volume: 18

Topics: Addison Disease; Adrenal Cortex Hormones; Amphetamines; Animals; Antidepressive Agents, Tricyclic; Bipolar Disorder; Brain; Cushing Syndrome; Cyclic AMP; Depression; Electroconvulsive Therapy; Humans; Lithium; Methyltyrosines; Monoamine Oxidase Inhibitors; Neurotransmitter Agents; Reserpine; Tryptophan

1975

Other Studies

2 other study(ies) available for tryptophan and Addison Disease

Article	Year
New insights into the molecular basis of the triple A syndrome. Endocrine research, 2002, Volume: 28, Issue:4 Topics: Addison Disease; Aspartic Acid; DNA Mutational Analysis; Esophageal Achalasia; Genotype; Heterozygote; Homozygote; Humans; Lacrimal Apparatus Diseases; Mutation; Nerve Tissue Proteins; Nuclear Pore Complex Proteins; Phenotype; Proteins; Repetitive Sequences, Amino Acid; Syndrome; Tryptophan	2002
The codon 620 tryptophan allele of the lymphoid tyrosine phosphatase (LYP) gene is a major determinant of Graves' disease. The Journal of clinical endocrinology and metabolism, 2004, Volume: 89, Issue:11 Topics: Addison Disease; Alleles; Codon; Graves Disease; Humans; Lymphocytes; Polymorphism, Single Nucleotide; Protein Tyrosine Phosphatase, Non-Receptor Type 1; Protein Tyrosine Phosphatases; Tryptophan	2004

Article

Year

New insights into the molecular basis of the triple A syndrome.

Endocrine research, 2002, Volume: 28, Issue:4

Topics: Addison Disease; Aspartic Acid; DNA Mutational Analysis; Esophageal Achalasia; Genotype; Heterozygote; Homozygote; Humans; Lacrimal Apparatus Diseases; Mutation; Nerve Tissue Proteins; Nuclear Pore Complex Proteins; Phenotype; Proteins; Repetitive Sequences, Amino Acid; Syndrome; Tryptophan

2002

The codon 620 tryptophan allele of the lymphoid tyrosine phosphatase (LYP) gene is a major determinant of Graves' disease.

The Journal of clinical endocrinology and metabolism, 2004, Volume: 89, Issue:11

Topics: Addison Disease; Alleles; Codon; Graves Disease; Humans; Lymphocytes; Polymorphism, Single Nucleotide; Protein Tyrosine Phosphatase, Non-Receptor Type 1; Protein Tyrosine Phosphatases; Tryptophan

2004