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المؤلفون: Dangouloff, Tamara, MOURAUX, Charlotte, Piazzon, Flavia, Mashhadizadeh, Davood, Hovhannesyan, Kristine, Helou, Laura, Palmeira, Leonor, Boemer, François, Servais, Laurent

المصدر: 33e Séminaire de Génétique Clinique, Angers, France [FR], 02 et 03 Février 2023

مصطلحات موضوعية: Human health sciences, Neurology, Sciences de la santé humaine, Neurologie

URL الوصول: https://orbi.uliege.be/handle/2268/300110

المؤلفون: Adoukonou, Thierry, Aryani, Omid, Barisic, Nina, Bashiri, Fahad, Bastaki, Laila, Benitto, Afaf, Omran, Tawfeg Ben, Bernert, Guenther, Bertini, Enrico, Borde, Patricia, Born, Peter, Boustani, Rose-Mary, Butoianu, Nina, Castiglioni, Claudia, Catibusic, Feriha, Chan, Sophelia, Chien, Yin Hsiu, Christodoulou, Kyproula, Dejsuphong, Donniphat, Farrar, Michelle, Filip, Duma, Goemans, Nathalie, Guinhouya, Kokou, Haberlova, Jana, Hadzsiev, Kinga, Hovhannesyan, Kristine, Isohanni, Pirjo, Radovic, Nelica Ivanovic, Jacquier, David, Jalloh, Alusine, Jedrzejowska, Maria, Kandawasvika, Gwen, Kaputu, Celestin, Kawatu, Nfwama, Kernohan, Kristin, Kirschner, Jan, Klink, Barbara, Kodsy, Sherry, Kouame-Assouan, Ange-Eric, Kravljanac, Ruzica, Kreile, Madara, Litvinenko, Ivan, McMillan, Hugh, Mesa, Sandra, Mohamed, Inaam, Kanzoska, Liljana Muaremoska, Nevo, Yoram, Nguefack, Seraphin, Nkole, Kafula, O'Grady, Gina, O'Rourke, Declan, Oskoui, Maryam, Piazzon, Flavia, Poddighe, Dimitri, Prasauskiene, Audrone, Prieto, Juan, Rasmussen, Magnhild, Razafindrasata, Santara, Saha, Narayan, Saito, Kayoko, Sakadi, Foksouna, Sangare, Modibo, Schroth, Mary, Shalkevich, Leanid, Shatillo, Andriy, Suthar, Renu, Szabo, Lena, Tatishvili, Nana, Tazir, Meriem, Tizzano, Eduardo, Topaloglu, Haluk, Tulinius, Mar, van der Pol, Ludo, Vazquez, Gabriel, Vlodavets, Dimitry, Wanigasinghe, Jithangi, Wilmshurst, Jo, Xiong, Hui, Zafeiriou, Dimitrios, Zamba, Eleni, Dangouloff, Tamara, Vrščaj, Eva, Servais, Laurent, Osredkar, Damjan

المصدر: In Neuromuscular Disorders June 2021 31(6):574-582

المؤلفون: PIAZZON, FLAVIA, Hovhannesyan, Kristine, Dangouloff, Tamara, Boemer, François, Sander, Stephan, Servais, Laurent

مصطلحات موضوعية: genetic 1st-tier newborn screening, Medical Sciences, medical genetics, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, molecular newborn screening, newborn screening, Diseases, Pediatrics, Medical Molecular Biology, Medicine and Health Sciences, Medical Specialties, Public Health, scoping review, treatable rare disorders

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::f5c7ba704cad521a66b681dc77d693fc

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المؤلفون: Hovhannesyan K; Center of Medical Genetics and Primary Health Care, Yerevan, Armenia. kristgen@yahoo.com., Sahakyan S; Turpanjian School of Public Health, American University of Armenia, Yerevan, Armenia., Davtyan K; FMD K & L, Yerevan, and TB Research and Prevention Center NGO, Yerevan, Armenia., Gasparyan S; FMD K & L, Yerevan, Armenia., Sarkisyan T; Center of Medical Genetics and Primary Health Care, Yerevan, Armenia., Reid AJ; Operational Research Unit, Operational Centre Brussels, Médecins sans Frontières, Luxembourg.

المصدر: Clinical and experimental rheumatology [Clin Exp Rheumatol] 2019 Nov-Dec; Vol. 37 Suppl 121 (6), pp. 154-155. Date of Electronic Publication: 2019 Mar 04.

نوع المنشور: Letter

بيانات الدورية: Publisher: Clinical And Experimental Rheumatology S.A.S Country of Publication: Italy NLM ID: 8308521 Publication Model: Print-Electronic Cited Medium: Print ISSN: 0392-856X (Print) Linking ISSN: 0392856X NLM ISO Abbreviation: Clin Exp Rheumatol Subsets: MEDLINE

مواضيع طبية MeSH: Familial Mediterranean Fever*/drug therapy , Familial Mediterranean Fever*/epidemiology, Armenia/epidemiology ; Humans