Autor: "Boduroğlu, K." - OpacWWW

Skocz do pozycji: 1.

Tytuł:: Three cases of spondyloenchondrodysplasia (SPENCD) with systemic lupus erythematosus: a case series and review of the literature.
Autorzy:: Bilginer Y; Department of Pediatrics, Division of Rheumatology, Hacettepe University Faculty of Medicine, Ankara, Turkey .
Düzova A; Department of Pediatrics, Division of Nephrology, Hacettepe University Faculty of Medicine, Ankara, Turkey.
Topaloğlu R; Department of Pediatrics, Division of Nephrology, Hacettepe University Faculty of Medicine, Ankara, Turkey.
Batu ED; Department of Pediatrics, Division of Rheumatology, Hacettepe University Faculty of Medicine, Ankara, Turkey.
Boduroğlu K; Department of Pediatrics, Division of Genetics, Hacettepe University Faculty of Medicine, Ankara, Turkey.
Güçer Ş; Department of Pediatrics, Division of Pathology, Hacettepe University Faculty of Medicine, Ankara, Turkey.
Bodur I; Department of Pediatrics, Division of Nephrology, Hacettepe University Faculty of Medicine, Ankara, Turkey.
Alanay Y; Department of Pediatrics, Pediatric Genetic Unit, Acıbadem University School of Medicine, İstanbul, Turkey.; Pokaż więcej
Źródło:: Lupus [Lupus] 2016 Jun; Vol. 25 (7), pp. 760-5. Date of Electronic Publication: 2016 Feb 06.
Typ publikacji:: Case Reports; Journal Article; Review
MeSH Terms:: Autoimmune Diseases/*complications
Autoimmune Diseases/*genetics
Lupus Erythematosus, Systemic/*complications
Osteochondrodysplasias/*complications
Osteochondrodysplasias/*genetics
Tartrate-Resistant Acid Phosphatase/*genetics
Adolescent ; Antibodies, Antinuclear/blood ; Child ; Child, Preschool ; Female ; Humans ; Lupus Nephritis/complications ; Magnetic Resonance Imaging ; Male ; Mutation
SCR Disease Name:: Spondyloenchondrodysplasia

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Skocz do pozycji: 2.

Tytuł:: Medical management of moyamoya disease and recurrent stroke in an infant with Majewski osteodysplastic primordial dwarfism type II (MOPD II).
Autorzy:: Kılıç E; Department of Pediatrics, Division of Pediatric Genetic, Hacettepe University Children's Hospital, 06100 Ankara, Turkey. />Utine E
Unal S
Haliloğlu G
Oğuz KK
Cetin M
Boduroğlu K
Alanay Y; Pokaż więcej
Źródło:: European journal of pediatrics [Eur J Pediatr] 2012 Oct; Vol. 171 (10), pp. 1567-71. Date of Electronic Publication: 2012 Apr 17.
Typ publikacji:: Case Reports; Journal Article
MeSH Terms:: Carbamazepine/*therapeutic use
Dwarfism/*complications
Heparin, Low-Molecular-Weight/*therapeutic use
Microcephaly/*complications
Moyamoya Disease/*drug therapy
Osteochondrodysplasias/*complications
Stroke/*drug therapy
Antigens/genetics ; Female ; Fetal Growth Retardation ; Humans ; Infant ; Magnetic Resonance Angiography ; Moyamoya Disease/complications ; Recurrence ; Stroke/etiology
SCR Disease Name:: Microcephalic Osteodysplastic Primordial Dwarfism, Type II

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