Search Results - "G.P."

Clinical Features and Familial Mutations in an Autosomal-Inherited Alport Syndrome Patient With the Presentation of Nephrotic Syndrome by Dahai Wang, Chunrong Shan, Xinxin Jing, Qiuye Zhang, Hong Chang, Yi Lin

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Albuminuria, cardiovascular risk factors and disease management in subjects with type 2 diabetes: a cross sectional study by Landgraf Rüdiger, Heier Margit, Meisinger Christa, Happich Michael, Wichmann H-Erich, Piehlmeier Wolfgang

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Necrotizing Funisitis as an Intrauterine manifestation of Cryopyrin-Associated Periodic Syndrome: a case report and review of the literature by Kyoko Yokoi, Sachiko Minamiguchi, Yoshitaka Honda, Mizuho Kobayashi, Satoru Kobayashi, Ryuta Nishikomori

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Diamour®, a newly vitrification device for human blastocysts, provides the same efficient perinatal outcomes as the commonly used Cryotop® by Masashi Yoshida, Shiori Abe, Yumi Koyanagi, Marina Nakano, Takao Miyake

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The influence of the type of embryo culture media on the outcome of IVF/ICSI cycles by Martin Stimpfel, Lili Bacer-Kermavner, Nina Jancar, Eda Vrtacnik-Bokal

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Feasibility and Compatibility of Minilaparotomy Hysterectomy in a Low-Resource Setting by Abhilasha Agarwal, Jyothi Shetty, Deeksha Pandey, Gazal Jain

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COMPOSIÇÃO CENTESIMAL, COMPOSTOS BIOATIVOS E PARÂMETROS FÍSICO-QUÍMICOS DO JENIPAPO (GENIPA AMERICANA L.) IN NATURA by Paula Pacheco, Josiane Gonçalves da Paz, Cassiano Oliveira da Silva, Grazieli Benedetti Pascoal

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Prevalence, risk factors and impact of proteinuria-associated hypomagnesemia in chronic kidney disease patients: cross-sectional study by Ayman Riyadh Abdel-Hameed, Mohammed Fouad Ahmed, Amr Ahmed Elsantawy, Maher Borai Mohammad

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A Matched Case Control Study of Surgically and Non-surgically Treated Patent Ductus Arteriosus in Extremely Pre-term Infants by Karl Wilhelm Olsson, Sawin Youssef, Mattias Kjellberg, Renske Raaijmakers, Richard Sindelar

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Whole exome sequencing revealed a novel homozygous variant in the DGKE catalytic domain: a case report of familial hemolytic uremic syndrome by Soraya Gholizad-kolveiri, Nakysa Hooman, Rasoul Alizadeh, Rozita Hoseini, Hasan Otukesh, Saeed Talebi, Mansoureh Akouchekian

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Admissions to a sick new born care unit in a secondary care hospital: Profile and outcomes by Ravi Shekhar Sinha, D Sharon Cynthia, P Vinod Kumar, Lois J Armstrong, Anuradha Bose, Kuryan George

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Syndrome of Congenital Insulin Resistance Caused by a Novel INSR Gene Mutation by Aleksandra Rojek, Beata Wikiera, Anna Noczynska, Marek Niedziela

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Anterior Minithoracotomy vs. Transcatheter Closure of Patent Ductus Arteriosus in Very Preterm Infants by Marien Lenoir, Chloé Wanert, Damien Bonnet, Damien Bonnet, Mathilde Méot, Barthélémy Tosello, Barthélémy Tosello, Virginie Fouilloux, Caroline Ovaert, Caroline Ovaert, Sophie Malekzadeh-Milani

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Ex Vivo COL7A1 Correction for Recessive Dystrophic Epidermolysis Bullosa Using CRISPR/Cas9 and Homology-Directed Repair by Araksya Izmiryan, Clarisse Ganier, Matteo Bovolenta, Alain Schmitt, Fulvio Mavilio, Alain Hovnanian

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Regular lung recruitment maneuvers during high-frequency oscillatory ventilation in extremely preterm infants: a randomized controlled trial by Tobias Werther, Erik Kueng, Lukas Aichhorn, Linda Pummer, Katharina Goeral, Angelika Berger, Michael Hermon, Katrin Klebermass-Schrehof

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Development of a Simple Dipstick Assay for Operational Monitoring of DDT. by Hanafy M Ismail, Vijay Kumar, Rudra P Singh, Christopher Williams, Pushkar Shivam, Ayan Ghosh, Rinki Deb, Geraldine M Foster, Janet Hemingway, Michael Coleman, Marlize Coleman, Pradeep Das, Mark J I Paine

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Characterization of a novel KCNJ2 sequence variant detected in Andersen-Tawil syndrome patients by Stefanie Scheiper, Brigitte Hertel, Britt-Maria Beckmann, Stefan Kääb, Gerhard Thiel, Silke Kauferstein

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Lack of association between mutation in IL36RN and palmoplantar pustular psoriasis in Chinese patients, by Yu Xiaoling, Shu Dan, Jin Hongzhong

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Detección de anomalías congénitas en 12.760 nacimientos de tres hospitales en la Ciudad de Bogotá, Colombia 2004-2005 mediante ecografía prenatal by Juan Camilo Gómez-Ruiz, Nicolás Fernández, Paola Páez, Ignacio Manuel Zarante

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Elevated IgA and IL-10 levels in very-early-onset inflammatory bowel disease secondary to IL-10 receptor deficiency by Natascha Silva Sandy, Lia Furlaneto Marega, Giane Dantas Bechara, Adriana Gut Lopes Riccetto, Carmen Bonfim, Maria Marluce dos Santos Vilela, Antonio Fernando Ribeiro, Maria De Fatima Servidoni, Elizete Aparecida Lomazi

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