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Search Results - Ozgurler, Funda
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A Hemophagocytic Lymphohistiocytosis Case with Newly Defined UNC13D (c.175G>C; p.Ala59Pro) Mutation and a Rare Complication
by
Balcı, Yasemin Işık
,
Özgürler Akpınar, Funda
,
Polat, Aziz
,
Kenar, Fethullah
,
Tesi, Bianca
,
Greenwood, Tatiana
,
Yalçın, Nagihan
,
Koçyiğit, Ali
Published in
Turkish journal of haematology
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The Roberts syndrome: a case report of an infant with valvular aortic stenosis and mutation in ESCO2
by
Dogan, Mustafa
,
Firinci, Fatih
,
Balci, Yasemin Isik
,
Zeybek, Selcan
,
Ozgürler, Funda
,
Erdogan, Ilkay
,
Varan, Birgül
,
Semerci, Cavidan Nur
Published in
Journal of the Pakistan Medical Association
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A 4-month-old infant with cough and fever
by
Firinci, Fatih
,
Ozgürler, Funda
,
Dogan, Mustafa
,
Devrim, Ilker
,
Nacaroglu, Tekin
,
Kocyigit, Ali
,
Mete, Emin
Published in
Pediatric annals
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Hereditary Spherocytosis and Wandering Spleen
by
Polat, Aziz
,
Ozgurler, Funda
,
Balc, Yasemin I k
,
Kocyigit, Ali
,
Tan, Metin
Published in
Pediatric hematology and oncology
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A Hemophagocytic Lymphohistiocytosis Case with Newly Defined UNC13D (c.175G>C; p.Ala59Pro) Mutation and a Rare Complication/Yeni Tanimlanan UNC13D (c.175G>C; p.Ala59Pro) Mutasyonlu...
by
Balci, Yasemin Isik
,
Akpinar, Funda Özgürler
,
Polat, Aziz
,
Kenar, Fethullah
,
Tesi, Bianca
,
Greenwood, Tatiana
,
Yalçin, Nagihan
,
Koçyigit, Ali
Published in
Turkish journal of haematology
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