Results 91 to 100 of about 28,339 (193)

Genetic Testing Unveils a Novel Thrombospondin‐1 Domain Containing Protein 1 Gene Variant as the Cause of Chronic Edema in a 79‐Year‐Old Woman

Clinical Genetics, EarlyView.
A 79‐year‐old woman with lifelong peripheral edema and an affected sister was found to harbor a novel homozygous THSD1 splice‐site variant. Reduced THSD1 expression in dermal endothelial cells supported the possibility that this variant contributes to chronic hereditary edema.
Eiko Amo, Takafumi Toyohara, Naoya Saijo, Satoko Sato, Jun Takayama, Yoshiko Suto, Yuji Noguchi, Sosuke Kinomura, Yusuke Ishizuka, Shun Watanabe, Koichi Kikuchi, Rui Makino, Mai Yoshida, Yuji Oe, Tasuku Nagasawa, Koji Okamoto, Takehiro Suzuki, Mariko Miyazaki, Shinya Kawaguchi, Takashi Suzuki, Takaaki Abe, Shigeo Kure, Atsuo Kikuchi, Tetsuhiro Tanaka   +23 more
wiley   +1 more source

Management of Congenital Complete Atrioventricular Block in Preterm Neonates With Novel Pacing Method

Pacing and Clinical Electrophysiology, EarlyView.
ABSTRACT Congenital complete atrioventricular block (CCAVB) is a rare autoimmune mediated disorder with a guarded prognosis, particularly when associated with extreme prematurity and severe bradycardia. Recent advances in neonatal care for extremely premature infants with delivery at level IV neonatal intensive care unit and novel pediatric pacing ...
Anusha Bai Kalithkar, Rodrigo Ruano, Leonardo Mulinari, Steven Fishberger, Sethuraman Swaminathan, Ileana Torres‐Burgos   +5 more
wiley   +1 more source

Congenital Skin Sloughing in the Setting of Hydrops Fetalis Secondary to Congenital Diffuse Lymphangiectasia Mimicking Epidermolysis Bullosa

Pediatric Dermatology, EarlyView.
ABSTRACT We present a case where the combination of severe hydrops fetalis, lymphangiectasia, and skin desquamation created a clinical picture that masqueraded as epidermolysis bullosa (EB). A neonate presented at birth with severe hydrops fetalis and extensive skin sloughing.
Sophia Rafferty, Kate L. Wilson, Jennifer B. Mancuso, Nicole Larsen, Grace A. Osborne, Jacqueline Meadow   +5 more
wiley   +1 more source

Protective effect of edaravone against endolymphatic hydrops

, 2007
CONCLUSION: Our findings suggest that edaravone prevented the production of reactive oxygen species (ROS). Edaravone also delayed the formation of endolymphatic hydrops in guinea pigs, but had no effect on endolymphatic hydrops. OBJECTIVE: To analyse the
Masaya Takumida, Akinori Kakigi, Nakatani, Hiroaki, Setsuko Takeda, Hiroaki Nakatani, Matti Anniko, Kakigi, Akinori, Taizo Takeda, Takumida, Masaya,, Takeda, Setsuko, Anniko, Matti,, Takeda, Taizo   +11 more
core   +1 more source

Ein Fall von Hydrops genu intermittens

, 1888
EIN FALL VON HYDROPS GENU INTERMITTENS Ein Fall von Hydrops genu intermittens ([1]) Binding ( - ) Title page ([1]) Dedication ([3]) Chapter ([5]) Section (23) Vita. ( - ) Thesen. ( - ) Binding ( -
Eschricht, Carl
core   +1 more source

Massive fetomaternal hemorrhage and successful prevention of maternal RhD alloimmunization: A case report

Transfusion, EarlyView.
Abstract Background Massive fetomaternal hemorrhage can lead to significant fetal morbidity or mortality. RhD negative patients require appropriate treatment to prevent alloimmunization in subsequent pregnancies. Few cases with follow‐up into future pregnancies have been reported.
Sajjad Hassan, Angela Essa, Lauren Orr, Corina N. Schoen, Chester Andrzejewski   +4 more
wiley   +1 more source

Hydrops Fetalis. [PDF]

Hydrops fetalis is a severe, life-threatening fetal condition, characterized by abnormal fluid accumulation in two or more fetal compartments. This thesis focuses on both immune and non-immune hydrops fetalis (NIHF), with the emphasis on the latter due ...
Rehmann, Felicitas,
core  

Drei Fälle von allgemeinem fötalem Hydrops

, 1887
DREI FÄLLE VON ALLGEMEINEM FÖTALEM HYDROPS Drei Fälle von allgemeinem fötalem Hydrops ([1]) Title page ([1]) Dedication ([3]) Chapter ([4]) Vita.
Hönck, Ernst
core   +1 more source

Mapping obstetric biobanks: A scoping review highlighting gaps in the study of alloimmunized pregnancies

Transfusion, EarlyView.
Abstract Background Maternal red cell alloimmunization can cause hemolytic disease of the fetus and newborn (HDFN), yet prediction of disease severity remains limited. Biobanks that link pregnancy biospecimens with clinical and laboratory data could accelerate translational research; however, the landscape of relevant obstetric biobanks has not been ...
Orlin Chowdhury, Chantal Armali, Catherine Devion, Sasha Kyser‐Burke, Akash Gupta, Noor Niyar N. Ladhani, Harley Meirovich, Hubert Tsui, Noah Zweig, Yulia Lin, Heather VanderMeulen   +10 more
wiley   +1 more source

Acute endolymphatic hydrops [PDF]

, 2005
De ziekte van Menière wordt gekenmerkt door aanvallen van draaiduizeligheid, wisselend gehoorverlies en oorsuizen. Ondanks het feit dat er al veel onderzoek is gedaan naar de oorzaak van deze ziekte, is nog veel onbekend.
Valk, Willem Laurens,, Valk, Willem Laurens   +1 more
core