valine and Hamartoma Syndrome, Multiple

valine has been researched along with Hamartoma Syndrome, Multiple in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Boespflug, A; Bringuier, PP; Couraud, S; Durieu, I; Edery, P; Gérinière, L; Isaac, S; Perrot, E; Souquet, PJ	1

Other Studies

1 other study(ies) available for valine and Hamartoma Syndrome, Multiple

Article	Year
Primary lung adenocarcinoma occurring in a PTEN related syndrome (Cowden's disease): routine EGFR sequencing also highlights two rare somatic mutations S768I and V769L. Lung cancer (Amsterdam, Netherlands), 2013, Volume: 79, Issue:3 Topics: Adenocarcinoma; Adult; Chromosome Disorders; Diagnosis, Differential; DNA Mutational Analysis; ErbB Receptors; Female; Germ-Line Mutation; Hamartoma Syndrome, Multiple; Humans; Lung Neoplasms; Phosphatidylinositol 3-Kinases; Proto-Oncogene Proteins c-akt; PTEN Phosphohydrolase; Serine; Signal Transduction; Valine	2013

Article

Year

Primary lung adenocarcinoma occurring in a PTEN related syndrome (Cowden's disease): routine EGFR sequencing also highlights two rare somatic mutations S768I and V769L.

Lung cancer (Amsterdam, Netherlands), 2013, Volume: 79, Issue:3

Topics: Adenocarcinoma; Adult; Chromosome Disorders; Diagnosis, Differential; DNA Mutational Analysis; ErbB Receptors; Female; Germ-Line Mutation; Hamartoma Syndrome, Multiple; Humans; Lung Neoplasms; Phosphatidylinositol 3-Kinases; Proto-Oncogene Proteins c-akt; PTEN Phosphohydrolase; Serine; Signal Transduction; Valine

2013