tryptophan and Severe Combined Immunodeficiency

tryptophan has been researched along with Severe Combined Immunodeficiency in 2 studies

Research

Studies (2)

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

Authors

Authors	Studies
CREPALDI, G; PARPAJOLA, A	1
Arrendondo-Vega, FX; Buckley, R; Conley, ME; El Dahr, J; Hershfield, MS; Notarangelo, LD; Roifman, C; Santisteban, I	1

Other Studies

2 other study(ies) available for tryptophan and Severe Combined Immunodeficiency

Article	Year
EXCRETION OF TRYPTOPHAN METABOLITES IN DIFFERENT FORMS OF HAEMOBLASTOSIS. Clinica chimica acta; international journal of clinical chemistry, 1964, Volume: 9 Topics: Cortisone; Cyclophosphamide; Genetic Diseases, X-Linked; Hodgkin Disease; Humans; Kynurenic Acid; Kynurenine; Leukemia; Leukemia, Hairy Cell; Leukemia, Lymphoid; Leukemia, Myeloid; Lymphatic Diseases; Lymphoma; Lymphoma, Large B-Cell, Diffuse; Lymphoma, Non-Hodgkin; Mechlorethamine; Multiple Myeloma; ortho-Aminobenzoates; Phenylbutazone; Polycythemia Vera; Proteins; Pyridoxal Phosphate; Pyridoxine; Sarcoma; Severe Combined Immunodeficiency; Tryptophan; Urine; Xanthurenates	1964
Seven novel mutations in the adenosine deaminase (ADA) gene in patients with severe and delayed onset combined immunodeficiency: G74C, V129M, G140E, R149W, Q199P, 462delG, and E337del. Mutations in brief no. 142. Online. Human mutation, 1998, Volume: 11, Issue:6 Topics: Adenosine Deaminase; Adolescent; Adult; Age of Onset; Arginine; Cysteine; Glutamic Acid; Glutamine; Glycine; Humans; Methionine; Mutation; Proline; Sequence Deletion; Severe Combined Immunodeficiency; Tryptophan; Valine	1998

Article

Year

EXCRETION OF TRYPTOPHAN METABOLITES IN DIFFERENT FORMS OF HAEMOBLASTOSIS.

Clinica chimica acta; international journal of clinical chemistry, 1964, Volume: 9

Topics: Cortisone; Cyclophosphamide; Genetic Diseases, X-Linked; Hodgkin Disease; Humans; Kynurenic Acid; Kynurenine; Leukemia; Leukemia, Hairy Cell; Leukemia, Lymphoid; Leukemia, Myeloid; Lymphatic Diseases; Lymphoma; Lymphoma, Large B-Cell, Diffuse; Lymphoma, Non-Hodgkin; Mechlorethamine; Multiple Myeloma; ortho-Aminobenzoates; Phenylbutazone; Polycythemia Vera; Proteins; Pyridoxal Phosphate; Pyridoxine; Sarcoma; Severe Combined Immunodeficiency; Tryptophan; Urine; Xanthurenates

1964

Seven novel mutations in the adenosine deaminase (ADA) gene in patients with severe and delayed onset combined immunodeficiency: G74C, V129M, G140E, R149W, Q199P, 462delG, and E337del. Mutations in brief no. 142. Online.

Human mutation, 1998, Volume: 11, Issue:6

Topics: Adenosine Deaminase; Adolescent; Adult; Age of Onset; Arginine; Cysteine; Glutamic Acid; Glutamine; Glycine; Humans; Methionine; Mutation; Proline; Sequence Deletion; Severe Combined Immunodeficiency; Tryptophan; Valine

1998