H Zhuang, A Alavi - Seminars in nuclear medicine, 2002 - Elsevier During the past decade, 18-fluorodeoxyglucose (FDG) positron emission tomography
(PET) has rapidly evolved from a pure research modality to a clinical necessity.
FDG-PET was introduced to determine the state of brain function in ... Cited by 209 - Related articles - BL Direct - All 11 versions
- ►nih.gov [PDF] C Cazeneuve, T Sarkisian, C Pêcheux, M … - The American Journal of Human Genetics, 1999 - Elsevier Familial Mediterranean fever (FMF) is a recessively inherited disorder that is
common in patients of Armenian ancestry. To date, its diagnosis, which can be
made only retrospectively, is one of exclusion, based entirely on ... Cited by 139 - Related articles - BL Direct - All 10 versions
- ►oxfordjournals.org F Yalcinkaya, N Cakar, M Misirlioglu, N … - Rheumatology, 2000 - Br Soc Rheumatology Objectives. Differences in clinical manifestations of familial Mediterranean
fever (FMF) between different ethnic groups have been documented. The FMF gene
was recently cloned and four missense mutations (Met694Val, Met680Ile, ... Cited by 61 - Related articles - BL Direct - All 5 versions
C Dode, C Pecheux, C Cazeneuve, D Cattan, … - American journal of medical genetics, 2000 - interscience.wiley.com Familial Mediterranean fever (FMF) is an autosomal recessively inherited disease
affecting patients of the Mediterranean basin. FMF is characterized by recurrent
episodes of fever accompanied with topical signs of inflammation. Some ... Cited by 57 - Related articles - BL Direct - All 3 versions
N Akar, M Misiroglu, F Yalcinkaya, E Akar, N … - Human Mutation, 2000 - interscience.wiley.com Familial Mediterranean fever (FMF) is a recessive inherited disorder affecting
Sephardic Jews, Arabs, Armenians and Turks. The gene responsible for FMF was
recently cloned and several disease-associated mutations have been ... Cited by 50 - Related articles - All 2 versions
- ►oxfordjournals.org HA Majeed, M Rawashdeh, H El-Shanti, H … - Qjm, 1999 - Oxford Univ Press The clinical picture of familial Mediterranean fever (FMF) has been appreciably
expanded in the last 10 years. Over 8 years, we studied the expanded clinical
profile of FMF in 476 children. Of these, 81% had abdominal pain, 41% chest ... Cited by 42 - Related articles - BL Direct - All 5 versions
- ►annals.org [PDF] A Simon, L Cuisset, MF Vincent, SD van der … - Annals of internal medicine, 2001 - Am Coll Physicians Molecular Analysis of the Mevalonate Kinase Gene in a Cohort of ... Patients
with the Hyper-IgD and Periodic Fever Syndrome: Its ... Anna Simon, MD;
Laurence Cuisset, PhD; M.-Françoise Vincent, PhD; Saskia D. van der Velde- ... Cited by 42 - Related articles - All 7 versions
A Pædiatrica - Acta Paediatrica - interscience.wiley.com It is also possible that your web browser is not configured or not able to
display style sheets. In this case, although the visual presentation will be
degraded, the site should continue to be functional. We recommend using the ... Cited by 36 - Related articles - BL Direct - All 7 versions
M Medlej-Hashim, M Rawashdeh, E Chouery, I … - Human Mutation, 2000 - interscience.wiley.com Familial Mediterranean fever is an autosomal recessive disorder characterised by
episodic fever, abdominal and pleuritic pain, serositis and arthritis. The FMF
gene (MEFV) has been mapped to chromosome 16p13.3 and generates a protein ... Cited by 32 - Related articles - All 2 versions
- ►bmj.com [PDF] K Konstantopoulos, A Kanta, C Deltas, V … - British Medical Journal, 2003 - ard.bmj.com Objective: To search for pyrin mutations associated with familial Mediterranean
fever (FMF) in Greece. Patients and methods: 62 patients fulfilling the Tel
Hashomer diagnostic criteria for definite (33) or probable (29) FMF ... Cited by 28 - Related articles - BL Direct - All 8 versions