نتایج جستجو برای: fetomaternal transfusion

تعداد نتایج: 31850  

2010
PUSHPA SIRICHAND

OBJECTIVE: To determine the maternal and perinatal complications in patients presented with antepartum hemorrhage (APH) at a tertiary care hospital so that a preventive strategy can be made to optimize fetomaternal outcome. METHODOLOGY: This prospective descriptive study was conducted from September 2007 to august 2008 at Department of Gynaecology and Obstetrics unit II, Liaquat University Hosp...

2016
JEAN UWINGABIYE HAFID ZAHID FAYÇAL LABRINI ABDELHAK EL KHAZRAJI ANASS YAHYAOUI RACHID HADEF NEZHA MESSAOUDI

We report a case of dramatic outcome of severe hemolytic disease in a newborn due to RH1 incompatibility. A newborn with A RH1 blood group was admitted in the Mohammed V Military Teaching Hospital for the problem of hydrops fetalis associated with RH1 incompatibility. The blood group of his mother, aged 31, was AB RH1-negative and that of his 37 year old father was A RH1. The mother had a histo...

Journal: :International Journal of Medical and Biomedical Studies 2020

Journal: :International Journal of Reproduction, Contraception, Obstetrics and Gynecology 2018

Journal: :Indian Journal of Obstetrics and Gynecology Research 2020

Journal: :The Australian & New Zealand journal of obstetrics & gynaecology 2011
Zoe K McQuilten Erica M Wood Helen Savoia Stephen Cole

Fetomaternal or neonatal alloimmune thrombocytopenia (NAIT) is a rare but serious condition associated with significant fetal and neonatal morbidity and mortality. The most useful predictor of severe disease is a history of a sibling with an antenatal intracranial haemorrhage. However, NAIT can occur during the first pregnancy and may not be diagnosed until the neonatal period. Antenatal treatm...

Journal: :Blood 2004
Ryuta Nishikomori Hiroshi Akutagawa Kyoko Maruyama Mami Nakata-Hizume Katsuyuki Ohmori Kazunori Mizuno Akihiro Yachie Takahiro Yasumi Takashi Kusunoki Toshio Heike Tatsutoshi Nakahata

X-linked ectodermal dysplasia and immunodeficiency (XL-EDA-ID) is an X-linked recessive disease caused by a mutation in the nuclear factor-kappaB (NF-kappaB) essential modulator (NEMO). Here we report an XL-EDA-ID patient with atypical features of very few naive-phenotype T cells and defective mitogen-induced proliferation of peripheral blood mononuclear cells (PBMCs). The patient's NEMO defect...

2014
Phelipe O Favaron João C Morini Andrea M Mess Maria A Miglino Carlos E Ambrósio

BACKGROUND Placental research in carnivores has concentrated on domestic species, which have zonary, labyrinthine placentas with an endotheliochorial barrier. Although the coati, Nasua nasua, is a widely distributed species in South America, data on the development of the placenta and the fetal membranes in this species are very sparse. FINDINGS Four placentas from mid-gestation to near term ...

Journal: :caspian journal of internal medicine 0
ebrahim alijanpour ali jabbari fahimeh hoseini shabnam tabasi

background: many of the multiple traumatized patients who refer to the hospital need transfusion. transfusion-related acute lung injury (trali) is a serious clinical syndrome associated with the transfusion of plasma-containing blood components. in the article, we present a case of trali following transfusion of packed red blood cells case presentation: a 24 year old male referred to shahid beh...

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