Search Results - "rare diseases"

Malignant Brenner tumor of the ovary: Case series and review of treatment strategies by Yingao Zhang, S. Allison Staley, Katherine Tucker, Leslie H. Clark

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Atypical hemolytic uremic syndrome precipitated by thyrotoxicosis: a case report by Ling Hou, Yue Du

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A Case of Late-onset Hyperinsulinemic Hypoglycemia: HNF4A Mutation by Gülçin Arslan, Sezer Acar, Taha Reşid Özdemir, Özlem Nalbantoğlu, Özgür Kırbıyık, Özge Köprülü, Beyhan Özkaya, Behzat Özkan

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Imunoglobulina intravenosa para tratamento de epidermólise bolhosa adquirida grave refratária a terapia imunossupressora convencional Intravenous immunoglobulin for treatment of se... by Carolina Balbi Mosqueira, Laura de Albuquerque Furlani, Augusto Frederico de Paula Xavier, Paulo Rowilson Cunha, Alda Maria Penna Galvão

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Considerations about the physical rehabilitation and physiotherapy on kinesiologic and functional alterations in a case of Endemic Pemphigus foliaceus - doi:10.5020/18061230.2007.p... by Carlos Hermano da Justa Pinheiro, Wilson Martins de Sousa Filho, Denise Gonçalves Moura Pinheiro, Ana Cristhina de Oliveira Brasil

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Effect of empowerment based on the Gibson model on self-efficacy and quality of life in the mothers of children with thalassemia by Yaser Shahsavari, Seyed Habibollah Hosseini, Ahmad Reza Sayadi, Tabandeh Sadeghi

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A case of severe malnutrition infant with neonatal onset intractable diarrhea by Youhong Fang, Youyou Luo, Jindan Yu, Jie Chen

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Neonatal congenital hyperinsulinism in Indonesia by I.Made Arimbawa, I.Wayan Eka Satriawibawa, Kadek Deddy Ariyanta, I.Made Darmajaya, Pande Putu Yuli Anandasari, Luh Putu Iin Indrayani Maker

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The impact of puberty on the onset, frequency, location, and severity of attacks in hereditary angioedema due to C1-inhibitor deficiency: A survey from the Italian Network for Here... by Mauro Cancian, Paola Triggianese, Stella Modica, Francesco Arcoleo, Donatella Bignardi, Luisa Brussino, Caterina Colangelo, Ester Di Agosta, Davide Firinu, Maria Domenica Guarino, Francesco Giardino, Marica Giliberti, Vincenzo Montinaro, Riccardo Senter

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Changes in Acute Poststreptococcal Glomerulonephritis: An Observation Study at a Single Korean Hospital Over Two Decades by Sueng-Woo Kuem, Sun-Mi Hur, You-Sook Youn, Jung-Woo Rhim, Jin-Soon Suh, Kyung-Yil Lee

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Molecular profiling of urinary extracellular vesicles in chronic kidney disease and renal fibrosis by Melanie Tepus, Elisa Tonoli, Elisabetta A. M. Verderio, Elisabetta A. M. Verderio

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Hemoglobinúria paroxística noturna e gravidez Paroxysmal nocturnal hemoglobinuria in pregnancy by Marcelo Luís Nomura, Fernanda Garanhani de Castro Surita, Mary Angela Parpinelli, Egle Cristina Couto Carvalho, Renato Passini Júnior

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Homozygous splice-site variant in ENPP1 underlies generalized arterial calcification of infancy by Hafiza Noor Ul Ayan, Yvonne Nitschke, Abdul Razzaq Mughal, Holger Thiele, Naveed Altaf Malik, Ijaz Hussain, Syed Muhammad Ijlal Haider, Frank Rutsch, Jeanette Erdmann, Muhammad Tariq, Zouhair Aherrahrou, Ilyas Ahmad

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Ovarian carcinosarcoma (a literature review) by A. M. Beishembaev, K. I. Zhordania, E. D. Choi, A. A. Turkmenov, A. K. Moldobekova

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A Rare Case Report of Neurological Condition: Moersch-Woltman Syndrome with Positive Anti-GAD Antibodies by Aakanksha Pitliya

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Recent Advances in Lipid Nanoparticles for Delivery of mRNA by Lei Yang, Liming Gong, Ping Wang, Xinghui Zhao, Feng Zhao, Zhijie Zhang, Yunfei Li, Wei Huang

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Clinical case of diagnosis of left ventricular non-compaction in a child by T.O. Kryuchko, S.M. Tanianska

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Evidence for long noncoding RNA GAS5 up-regulationin patients with Klinefelter syndrome by Michele Salemi, Rossella Cannarella, Rosita A. Condorelli, Laura Cimino, Federico Ridolfo, Giorgio Giurato, Corrado Romano, Sandro La Vignera, Aldo E. Calogero

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Expression of Low Affinity Nerve Growth Factor Receptor p75 in Classic Bladder Exstrophy by Martin Promm, Wolfgang Otto, Florian Weber, Stefanie Götz, Maximilian Burger, Karolina Müller, Peter Rubenwolf, Peter Rubenwolf, Winfried Neuhuber, Wolfgang H. Roesch

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Neonatal systemic juvenile Xanthogranuloma with Hydrops diagnosed by Purpura skin biopsy: a case report and literature review by Yohji Uehara, Yuka Sano Wada, Yuka Iwasaki, Kota Yoneda, Yasuhisa Ikuta, Shoichiro Amari, Hidehiko Maruyama, Keiko Tsukamoto, Tetsuya Isayama, Kenichi Sakamoto, Yoko Shioda, Osamu Miyazaki, Rie Irie, Takako Yoshioka, Naoko Mochimaru, Kazue Yoshida, Yushi Ito

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