MEFV gene mutations in Egyptian children with Henoch-Schonlein purpura
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H. Marzouk | S. Rizk | Y. Farag | S. Salah | H. Lotfy | Salma Z. El Houchi
[1] M. Al-Haggar,et al. Phenotype-genotype updates from familial Mediterranean fever database registry of Mansoura University Children’ Hospital, Mansoura, Egypt , 2014, Indian journal of human genetics.
[2] A. Ensari,et al. MEFV gene mutations in Henoch–Schönlein purpura , 2013, International journal of rheumatic diseases.
[3] M. Koyun,et al. Prevalence and significance of the MEFV gene mutations in childhood Henoch–Schönlein purpura without FMF symptoms , 2013, Rheumatology International.
[4] Mohamed A Gomaa,et al. The expanded clinical profile and the efficacy of colchicine therapy in Egyptian children suffering from familial mediterranean fever: a descriptive study , 2012, Italian Journal of Pediatrics.
[5] M. Houshmand,et al. MEFV gene mutations (M694V, V726A, M680I, and A744S) in Iranian children with Henoch-Schönlein purpura. , 2012, Pneumologia.
[6] H. El-Shanti,et al. Spectrum of mutations and carrier frequency of familial Mediterranean fever gene in the Algerian population. , 2011, Rheumatology.
[7] M. Bülbül,et al. Prevalence of MEFV gene mutations and their clinical correlations in Turkish children with Henoch–Schönlein purpura , 2011, Acta paediatrica.
[8] K. Aksu,et al. Coexistence of vasculitides with Familial Mediterranean Fever , 2011, Rheumatology International.
[9] C. Heng,et al. MEFV E148Q polymorphism is associated with Henoch–Schönlein purpura in Chinese children , 2010, Pediatric Nephrology.
[10] A. Bakkaloğlu,et al. EULAR/PRINTO/PRES criteria for Henoch–Schönlein purpura, childhood polyarteritis nodosa, childhood Wegener granulomatosis and childhood Takayasu arteritis: Ankara 2008. Part II: Final classification criteria , 2010, Annals of the rheumatic diseases.
[11] A. Bagga,et al. EULAR/PRINTO/PRES criteria for Henoch-Schönlein purpura, childhood polyarteritis nodosa, childhood Wegener granulomatosis and childhood Takayasu arteritis: Ankara 2008. Part I: Overall methodology and clinical characterisation , 2010, Annals of the rheumatic diseases.
[12] D. Hashad,et al. MEFV gene mutations in Egyptian patients with familial Mediterranean fever. , 2010, Genetic testing and molecular biomarkers.
[13] M. Fawzy,et al. Analysis of common MEFV mutations in Egyptian patients with familial Mediterranean fever: molecular characterisation of the disease , 2010, British journal of biomedical science.
[14] Sherif N. Amin,et al. MEFV mutations in Egyptian patients suffering from familial Mediterranean fever: analysis of 12 gene mutations , 2010, Rheumatology International.
[15] F. Yalçınkaya,et al. MEFV Mutations Modify the Clinical Presentation of Henoch-Schönlein Purpura , 2008, The Journal of Rheumatology.
[16] A. Bakkaloğlu,et al. Prevalence of the MEFV gene mutations in childhood polyarteritis nodosa. , 2007, The Journal of pediatrics.
[17] M. Lidar,et al. Familial Mediterranean fever: clinical, molecular and management advancements. , 2007, The Netherlands journal of medicine.
[18] A. Settin,et al. Clinical and molecular diagnosis of Familial Mediterranean Fever in Egyptian children. , 2007, Journal of gastrointestinal and liver diseases : JGLD.
[19] F. Saulsbury. Clinical update: Henoch-Schönlein purpura , 2007, The Lancet.
[20] A. Mégarbané,et al. Familial Mediterranean fever in the Syrian population: gene mutation frequencies, carrier rates and phenotype-genotype correlation. , 2006, European journal of medical genetics.
[21] R. Gershoni-baruch,et al. Prevalence and significance of mutations in the familial Mediterranean fever gene in Henoch-Schönlein purpura. , 2003, The Journal of pediatrics.
[22] C. Cazeneuve,et al. Clinical evaluation of a reverse hybridization assay for the molecular detection of twelve MEFV gene mutations. , 2003, Clinical chemistry.
[23] M. Tayeh,et al. Familial Mediterranean fever mutation frequencies and carrier rates among a mixed Arabic population. , 2003, Saudi medical journal.
[24] A. Bakkaloğlu,et al. Mutations in the gene for familial Mediterranean fever: do they predispose to inflammation? , 2003, The Journal of rheumatology.
[25] M. Hiratsuka,et al. Allele and genotype frequencies of polymorphic cytochromes P450 (CYP2C9, CYP2C19, CYP2E1) and dihydropyrimidine dehydrogenase (DPYD) in the Egyptian population. , 2002, British journal of clinical pharmacology.
[26] F. Saulsbury. Epidemiology of Henoch-Schönlein purpura. , 2002, Cleveland Clinic journal of medicine.
[27] M. Tekin,et al. Clinical, laboratory and molecular characteristics of children with Familial Mediterranean Fever‐associated vasculitis , 2000, Acta paediatrica.