Search Results - "Brothers

Clinical and molecular findings in a Chinese family with a de novo mitochondrial A1555G mutation by Ping Gu, Guojian Wang, Xue Gao, Dongyang Kang, Pu Dai, Shasha Huang

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Influence of Family Function about Youth Dependence to Synthetic Drugs by Mehdi Mirzaei Alavijeh, Mostafa Nasirzadeh, Ahmad Ali Eslami, GHolamreza Sharifirad, Akbar Hasanzadeh

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Late-onset dyshormonogenic goitrous hypothyroidism due to a homozygous mutation of the SLC26A7 gene: a case report by Elisabetta Sciarroni, Lucia Montanelli, Caterina Di Cosmo, Brunella Bagattini, Simone Comi, Luisa Pignata, Alessandro Brancatella, Giuseppina De Marco, Eleonora Ferrarini, Chiara Nencetti, Maria Rita Sessa, Francesco Latrofa, Ferruccio Santini, Massimo Tonacchera, Patrizia Agretti

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Case Report: A Case Study on the Neurodevelopmental Profile of a Child With Pallister-Killian Syndrome and His Unaffected Twin by Carole A. Samango-Sprouse, Carole A. Samango-Sprouse, Carole A. Samango-Sprouse, Mary P. Hamzik, Kenneth Rosenbaum, Kosar Khaksari, Francie Mitchell, Ritika Kommareddi, Michaela R. Brooks, Elizabeth Tipton, Teresa Sadeghin, Andrea L. Gropman, Andrea L. Gropman

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Allogeneic Hematopoietic Stem Cell Transplantation for PEX1-Related Zellweger Spectrum Disorder: A Case Report and Literature Review by Kai Chen, Na Zhang, Jing-Bo Shao, Hong Li, Jie Li, Jia-Ming Xi, Wu-Hen Xu, Hui Jiang

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Huma Betang's philosophical values in the character of Dayak cultural communication by Rico Rico, Muzahid Akbar Hayat, Khuzaini Khuzaini, Sanusi Sanusi, Didi Susanto

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A truncating variant altering the extreme C-terminal region of desmoplakin (DSP) suggests the crucial functional role of the region: a case report study by Malena P. Pantou, Polyxeni Gourzi, Vasiliki Vlagkouli, Efstathios Papatheodorou, Alexandros Tsoutsinos, Eva Nyktari, Dimitrios Degiannis, Aris Anastasakis

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Prevention of Identity Politics Through Multicultural Education by Nimas Permata Putri, Agoes Hendriyanto

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Novel HAX1 Gene Mutation in a Vietnamese Boy with Severe Congenital Neutropenia by Tham Thi Tran, Quang Van Vu, Taizo Wada, Akihiro Yachie, Huong Le Thi Minh, Sang Ngoc Nguyen

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Two fetuses in one family of arterial tortuosity syndrome: prenatal ultrasound diagnosis by Meiling Liang, Huaxuan Wen, Shengli Li

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Enzyme Replacement Therapy (ERT) on Heart Function Changes the Outcome in Patients with Infantile-Onset Pompe Disease: A Familial History by Marco Lecis, Katia Rossi, Maria Elena Guerzoni, Ilaria Mariotti, Lorenzo Iughetti

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A rare presentation of measles and post-measles complications in a neonate: case report by Suraksha Ramakrishna Sharma, Vishal Sawant, Sushma Uttam Save, Alpana Santosh Kondekar

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Do not ignore multiple capillary malformations in a child by Joana Calvão, Pedro Maia-Almeida, Leonor Ramos

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Prenatal Diagnosis of Rare Familial Unbalanced Translocation of Chromosomes 7 and 12 by Berrin Tezcan, Foteini Emmanouella Bredaki

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Cleidocranial dysplasia with growth hormone deficiency: a case report by Nozomi Takaki, Jun Mori, Satoshi Matsuo, Toshio Osamura, Toshimi Michigami

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Identification of a novel PTH1R variant in a family with primary failure of eruption by Yunchen Zha, Shushu Li, Yue-lin Yu, Zicheng Huang, Hai-ying Zhang, Weidong Kong

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Pseudoxanthoma elasticum and reflectance confocal microscopy: report of two affected young sisters by Victor Desmond Mandel, Federica Boraldi, Giovanni Pellacani, Silvana Ciardo, Giovanna Mazzaglia, Francesca Farnetani

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A Case of Hereditary Spherocytosis Initially Manifested as an Aplastic Crisis Caused by Parvovirus B19 Infection by Hyungsuk Jin, Ji Won Lee, Hee Young Ju, Hee Won Cho, Ju Kyung Hyun, Ki Woong Sung, Hong Hoe Koo, Hee-Jin Kim, Keon Hee Yoo

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Hydrometrocolpos in Infants: Etiologies and Clinical Presentations by Mi-Chi Chen, Yao-Lung Chang, Hsun-Chin Chao

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Strategi Pembelajaran Guru dalam Meningkatkan Mutu Belajar Siswa di Madrasah Aliyah Negeri Karo by Inom Nasution, Yuni Syafriani, Suci Ramadhani, Anggun Sari Fadilla, Dawi Nurjannah, Yogi Andrian, Imam Amir Musthofa, Sandy Franata Tarigan

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