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alanine and von Hippel-Lindau Disease

alanine has been researched along with von Hippel-Lindau Disease in 1 studies

Alanine: A non-essential amino acid that occurs in high levels in its free state in plasma. It is produced from pyruvate by transamination. It is involved in sugar and acid metabolism, increases IMMUNITY, and provides energy for muscle tissue, BRAIN, and the CENTRAL NERVOUS SYSTEM.
alanine : An alpha-amino acid that consists of propionic acid bearing an amino substituent at position 2.

von Hippel-Lindau Disease: An autosomal dominant disorder caused by mutations in a tumor suppressor gene. This syndrome is characterized by abnormal growth of small blood vessels leading to a host of neoplasms. They include HEMANGIOBLASTOMA in the RETINA; CEREBELLUM; and SPINAL CORD; PHEOCHROMOCYTOMA; pancreatic tumors; and renal cell carcinoma (see CARCINOMA, RENAL CELL). Common clinical signs include HYPERTENSION and neurological dysfunctions.

Research Excerpts

ExcerptRelevanceReference
"All patients were diagnosed as VHL syndrome type 2B."1.40Clinical presentation of Von Hippel Lindau syndrome type 2B associated with VHL p.A149S mutation in a large Turkish family. ( Aydin, Y; Berker, D; Ciliz, D; Guler, S; Mete, T; Onen, M; Ozgen, G; Tuna, M; Yalcin, Y; Yilmaz, E, 2014)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Mete, T1
Berker, D1
Yilmaz, E1
Ozgen, G1
Yalcin, Y1
Tuna, M1
Ciliz, D1
Onen, M1
Aydin, Y1
Guler, S1

Other Studies

1 other study available for alanine and von Hippel-Lindau Disease

ArticleYear
Clinical presentation of Von Hippel Lindau syndrome type 2B associated with VHL p.A149S mutation in a large Turkish family.
    Endocrine, 2014, Volume: 45, Issue:1

    Topics: Adolescent; Adult; Alanine; Amino Acid Substitution; Family; Female; Humans; Male; Middle Aged; Muta

2014