Search Results - "rare diseases"

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  1. 1401
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    Ectopic teeth in a patient with Gorham-Stout disease previously treated by biphosphonates: a case report by Le Donne Mélanie, Jaby Philippe, Farge Pierre, Gleizal Arnaud

    Published 2020
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  2. 1402
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    Recurrent hemolytic uremic syndrome caused by gene mutation: a case report by Baek Sup Shin, Yo Han Ahn, Hee Gyung Kang

    Published 2022
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  3. 1403
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    Two novel mutations in ADAMTS13 in a Chinese boy with congenital thrombocytopenic purpura: a case report by Ling Hou, Yue Du

    Published 2020
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  4. 1404
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    Miescher's granulomatosis (granulomatosis disciformis chronica et progressiva) in a non-diabetic patient - case report by Brzezińska-Wcisło Ligia, Bergler-Czop Beata, Rogala-Poborska Iwona

    Published 2009
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  5. 1405
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    Argyria mimicking a blue nevis: dermoscopy features Argyria imitando um nevo azul: características dermatoscópicas by Maria Leonor Enei, Francisco Macedo Paschoal, Rodrigo Valdés

    Published 2013
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  6. 1406
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    Artrogripose renal colestática diagnosticada a partir de colestase neonatal: relato de caso by Bruna Caseri Marino, Natascha Silva Sandy, Gabriel Hessel, Maria Angela Bellomo Brandão

    Published 2022
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  7. 1407
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    Aplasia cutis congenita on the scalp: case report and review of literature by Tiago Lima Castro, Carolina Garcia Pereira, Queila Esteves de Oliveira, Leandro Meirelles Nunes

    Published 2023
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  8. 1408
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    Clinical manifestations, toxicities, and outcome of two children with Nijmegen breakage syndrome and lymphoid malignancies - case reports by Aleksandra Filipiuk, Agata Kozakiewicz, Kamil Kośmider, Katarzyna Karska, Monika Lejman, Joanna Zawitkowska

    Published 2022
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  9. 1409
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    New daily persistent headache with isolated sphenoiditis in children by Jeongho Lee, Minhee Rhee, Eun Sook Suh

    Published 2015
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  10. 1410
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    Rare Case Report on Hydatid Cyst of Breast by Kassahun Tadele A, Israel Korga T, Melis Nisiro A, Abebe Ayele S

    Published 2022
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  11. 1411
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    Primary extrahepatic alveolar echinococcosis of the lumbar spine and the psoas muscle by Gradinger Reiner, da Costa Clarissa, Trappe Dennis, Schaeffeler Christoph, von Eisenhart-Rothe Rüdiger, Gradl Guntmar, Burgkart Rainer H, Nell Manuel, Kirchhoff Chlodwig

    Published 2011
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  12. 1412
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    Genetic dissection of a cell-autonomous neurodegenerative disorder: lessons learned from mouse models of Niemann-Pick disease type C by Manuel E. Lopez, Matthew P. Scott

    Published 2013
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  13. 1413
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    Amelogenesis imperfecta: therapeutic strategy from primary to permanent dentition across case reports by Steve Toupenay, Benjamin Philippe Fournier, Marie-Cécile Manière, Chantal Ifi-Naulin, Ariane Berdal, Muriel de La Dure- Molla

    Published 2018
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  14. 1414
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    Ramsay Hunt syndrome in a child - case report by Joanna Grabowska, Anna Ankudowicz, Grzegorz K. Ankudowicz

    Published 2016
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  15. 1415
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    Multiple primary cutaneous plasmacytoma: first reported case in Brazil Plasmocitoma cutâneo primário múltiplo: primeiro caso relatado no Brasil by Thais Lima Saback, Luciane Francisca Fernandes Botelho, Milvia Maria Simões da Silva Enokihara, Nilceo Schwery Michalany, Marcos César Floriano

    Published 2012
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  16. 1416
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    A Review on Acute Pediatric Pancreatitis by Hasan Karami, Mojdeh Dabirian

    Published 2016
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  17. 1417
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    Early-Onset Isolated Bilateral Pheochromocytoma As a Major Clinical Manifestation of von-Hippel Lindau Syndrome Type 2C by Sezer Acar, Hale Tuhan, Korcan Demir, Ayça Aykut, Asude Durmaz, Ünal Utku Karaarslan, Gözde İnci, Oğuz Ateş, Ece Böber, Ayhan Abacı

    Published 2018
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  18. 1418
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    Langerhans cell histiocytosis; an institutional study by Shovana Karki, Aasia Rajbhandari

    Published 2017
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  19. 1419
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    Comorbid Cardiovascular Malformation and Type II Mucolipidosis: Clinical Case by Nina V. Fedorova, Natalia V. Zhurkova, Nato D. Vashakmadze, Marina A. Babaykina, Grigory V. Revunenkov, Kirill V. Savostyanov, Olga B. Gordeeva, Leyla S. Namazova-Baranova

    Published 2020
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  20. 1420
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    Difficult diagnosis and genetic analysis of fibrodysplasia ossificans progressiva: a case report by Shengjie Tian, Jianhua Zhu, Yaogang Lu

    Published 2018
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