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  • Tag › enzyme replacement therapy

     Gaucher type 1 in pediatric practice: clinical observations

    Редактор | 2025, Practical medicine part 23 №3. 2025, СLINICAL OBSERVATIONS | 18 июня, 2025

    G.P. SMIRNOVA1, 2, S.N. DURYAGINA2, YU.V. SMORODINA2, I.A. KARATAEVA2, D.S. IVANOVA1, YU.S. SEKAREVA1  1Northern State Medical University, Arkhangelsk 2Arkhangelsk Children’s Clinical Hospital named after P.G. Vyzhletsov, Arkhangelsk Contact details: Smirnova G.P. — PhD (Medicine), Associate Professor of the Department of Pediatrics Address: 51 Troitsky prospekt, 163069 Arkhangelsk, Russian Federation, tel.: +7-902-194-87-39, e-mail: sovas1962@gmail.com Gaucher disease is […]

    Tag: 2025, Children, cytopenia, D.S. IVANOVA, enzyme replacement therapy, G.P. SMIRNOVA, Gaucher disease, glucocerebrosidase deficiency, hepatosplenomegaly, I.A. KARATAEVA, non-neuronopathic type, Practical medicine part 23 №3. 2025, S.N. DURYAGINA, YU.S. SEKAREVA, YU.V. SMORODINA
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    Mucopolysaccharidosis type I: diagnosis and treatment

    adm | 2013, Lectures for doctors, Practical medicine 06 (13) Pediatrics | 25 ноября, 2013

    S.Ya. VOLGINA Kazan State Medical University Volgina Svetlana Yakovlevna Doctor of Medical Science, Professor of Department of Hospital Pediatrics with courses of outpatient pediatrics and postgraduate education 75 Yamasheva avenue, apt.170, Kazan 420120 Tel. 8-904-671-16-59, e-mail: volgina_svetlana@mail.ru Mucopolysaccharidosis type I (MPS I) is a lysosomal storage disease. There are two forms of the disease — […]

    Tag: Children, enzyme replacement therapy, hematopoetic stem cell transplantation, mucopolysaccharidosis type I, Practical medicine 06 (13) Pediatrics
    Комментарии к записи Mucopolysaccharidosis type I: diagnosis and treatment отключены
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