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Publications by N Petrucelli
Variable Expressivity of Familial Medullary Thyroid Carcinoma (FMTC) Due to a RET V804M (GTGG→ATG) Mutation in Two Families: Reluctance of Gene Carriers to Accept Prophylactic Thyroidectomy
Genetics in Medicine
Medicine
Genetics
Related publications
Variable Expressivity of Osteogenesis Imperfecta in a Brazilian Family Due to p.G1079S Mutation in the COL1A1 Gene
Genetics and Molecular Research
Medicine
Genetics
Molecular Biology
RET Mutation p.S891A in a Chinese Family With Familial Medullary Thyroid Carcinoma and Associated Cutaneous Amyloidosis Binding OSMR Variant p.G513D
Oncotarget
Oncology
Editorial: Familial Medullary Carcinoma of the Thyroid.
BMJ
Over-Representation of a Germline RET Sequence Variant in Patients With Sporadic Medullary Thyroid Carcinoma and Somatic RET Codon 918 Mutation
Oncogene
Cancer Research
Genetics
Molecular Biology
3 Cases of Familial Medullary Carcinoma of the Thyroid
The journal of the Japanese Practical Surgeon Society
Medullary Thyroid Carcinoma: Genetic Screening and Prophylactic Thyroidectomies
Acta chirurgica iugoslavica
Early or Prophylactic Thyroidectomy in MEN 2/FMTC Gene Carriers: Results in 71 Thyroidectomized Patients. The French Calcitonin Tumours Study Group (GETC)
European Journal of Endocrinology
Medicine
Endocrinology
Metabolism
Diabetes
Emergence of a RET V804M Gatekeeper Mutation During Treatment With Vandetanib in RET-Rearranged NSCLC
Journal of Thoracic Oncology
Medicine
Oncology
Respiratory Medicine
Pulmonary
Discovery of Wt RET and V804M RET Inhibitors: From Hit to Lead
ChemMedChem
Organic Chemistry
Molecular Medicine
Pharmacology
Biochemistry
Toxicology
Drug Discovery
Pharmaceutics
