Search Results - "defection"

Accelerators of Osteogenesis by Recombinant Human Bone Morphogenetic Protein-2 by Yasunori Okubo, Kenji Kusumoto, Kazuhisa Bessho

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Goldenhar Syndrome in a 6-Year-Old Patient: a Case Report and Review of Literature by Fatemeh Jahanimoghadam, Maryam Sharifi

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The stages of examination, diagnosis and correction of pectus excavatum in children by M.O. Kaminska, V.A. Dihtiar

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Candidates Cell Sources to Regenerate Alveolar Bone from Oral Tissue by Masahiro Nishimura, Kazuma Takase, Fumio Suehiro, Hiroshi Murata

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Topical Issues of Modern Medical Care of Children of School Age in Ukraine by S.V. Krasnozhon

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Management of true lateral infected radicular cyst as well as associated mucosal fenestration that occurred postoperatively through an interdisciplinary approach: A rare case repor... by Sanjeev Kumar Salaria, Shashank Arora, Shefali Goyal, Amit Khunger

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Uterine rupture in a gravid, unscarred uterus: A case report by S.D. Halassy, J. Eastwood, J. Prezzato

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The role of nutrigenetics in diet personalisation by Karolina Rogulska, Aleksandra Strońska, Konrad Grzeszczak

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Rehabilitation of a hemimaxillectomy patient having microstomia with two-piece hollow obturator by Faisal Khan, Sunil Kumar Mishra

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Drugs and nonsyndromic orofacial cleft: an update by Annalisa Palmieri, Anna Avantaggiato, Giorgio Brunelli Marzia Arlotti, Luca Scapoli, Marcella Martinelli, Furio Pezzetti, Francesco Carinci

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Antibody-drug conjugates: Recent advances in linker chemistry by Zheng Su, Dian Xiao, Fei Xie, Lianqi Liu, Yanming Wang, Shiyong Fan, Xinbo Zhou, Song Li

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FUN14 Domain Containing 1 (FUNDC1): A Promising Mitophagy Receptor Regulating Mitochondrial Homeostasis in Cardiovascular Diseases by Yu Mao, Jun Ren, Jun Ren, Lifang Yang

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Clinical and molecular analysis of Noonan syndrome in Indonesia: a case report by Iffa Mutmainah, Willy Nillesen, Farmaditya Mundhofir, Tri Winarni, Ineke van der Burgt, Helger Yntema, Sultana Faradz

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Diagnostic and Management Issues in Patients with Late-Onset Ornithine Transcarbamylase Deficiency by Majitha Seyed Ibrahim, Jessica I. Gold, Alison Woodall, Berna Seker Yilmaz, Paul Gissen, Karolina M. Stepien

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Anterior cervical hypertrichosis with linear and whorled nevoid hypermelanosis in a 12-year-old girl: A rare association by Shivani Saini, Ramesh Kumar, Devendra Yadav

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Supraglottic devices as alternative equipment to airway management in state of sudden cardiac arrest by Rafał Czyż, Mateusz Zawłodzki, Izabela Czyż

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How Not to Miss the Mild Forms of Mucopolysaccharidosis Type I in Patients With Articular Manifestations of the Disease? by Natalia V. Buchinskaya, Mikhail M. Kostik, Oksana L. Kolobova, Larisa N. Melnikova

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Spectrum of Genetic Autoinflammatory Diseases Presenting with Cutaneous Symptoms by Hanna Bonnekoh, Monique Butze, Tilmann Kallinich, Naotomo Kambe, Georgios Kokolakis, Karoline Krause

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Animal models of vitiligo: Matching the model to the question by Kingsley I. Essien, John E. Harris

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Alveolar bone tissue engineering using composite scaffolds for drug delivery by Tomonori Matsuno, Kazuhiko Omata, Yoshiya Hashimoto, Yasuhiko Tabata, Tazuko Satoh

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