Rezultati pretrage - "Neurofibromatosis type I"

Plexiform Neurofibroma of the Larynx in Children: About an Unusual Case Report od R Mahdoufi, I Barhmi, N Tazi, R Sami, R Abada, M Roubal, M Mahtar

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Neurofibroma of the maxillary antrum: A rare case od Deepali Jain, Minal Chaudhary, Swati Patil

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Arteriovenous malformation underlying a plexiform neurofibroma: An unusual presentation od Zaheer Abbas, Sepideh Khani, Javad Zare

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An isolated colonic neurofibroma: A rare colonic neoplasm. Case report with clinicopathologic features and review of literature od Mukund Tinguria

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Malignant Peripheral Nerve Sheath Tumors-A Comprehensive Review of Pathophysiology, Diagnosis, and Multidisciplinary Management od Samantha W. E. Knight, Tristan E. Knight, Teresa Santiago, Andrew J. Murphy, Abdelhafeez H. Abdelhafeez

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Malignant peripheral nerve sheath tumor with rhabdoid features arising in the temporal region of a patient suffering from neurofibromatosis 1 - A case report od Hatem Wael Amer, Hamed Abdelwahab Shaheen, Madiha Nabil Ashoub, Sarah Ahmed Mohamed Mahmoud

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Uncommon presentation of a common histiocytic tumor: A rare entity od Chinmay Kar, Kapildev Das, Jayanta K Barua

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Plexiform Neurofibroma Treated with Pharmacopuncture od Chungsan Lim, Kirok Kwon, Kwangho Lee

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Florid cemento-osseous dysplasia and peripheral giant cell granuloma in a patient with neurofibromatosis 1 od Dmitry José de Santana Sarmento, Sérgio Henrique Gonçalves de Carvalho, José Cadmo Wanderley Peregrino de Araújo Filho, Marianne de Vasconcelos Carvalho, Éricka Janine Dantas da Silveira

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Central precocious puberty in a girl with LEGIUS syndrome: an accidental association? od Valentina Orlandi, Paolo Cavarzere, Laura Palma, Rossella Gaudino, Franco Antoniazzi

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A novel NF1 mutation in a pediatric patient with renal artery aneurysm od Ilenia Chillura, Giulia Angela Restivo, Simonetta Callari, Sabrina Cibella, Maria Michela D'Alessandro, Ciro Corrado, Mario Vallone, Vincenzo Antona, Giovanni Corsello

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LZTR1 molecular genetic overlap with clinical implications for Noonan syndrome and schwannomatosis od Kirsten M. Farncombe, Emily Thain, Carolina Barnett-Tapia, Hamid Sadeghian, Raymond H. Kim

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Correlation between large rearrangements and patient phenotypes in NF1 deletion syndrome: an update and review od Laurence Pacot, Milind Girish, Samantha Knight, Gill Spurlock, Vinod Varghese, Manuela Ye, Nick Thomas, Eric Pasmant, Meena Upadhyaya

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ENFERMEDAD DE VON RECKLINGHAUSEN Y EMBARAZO od Gregorio Evans M., Ronald Poulsen R., Cristián Mardones S.

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Four-year follow-up study in a NF1 Boy with a focal pontine hamartoma od Parisi Pasquale, Persechino Severino, Paolino Maria Chiara, Nicita Francesco, Torrente Isabella, Bozzao Alessandro, Villa Maria Pia

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RASopathies - what they reveal about RAS/MAPK signaling in skeletal muscle development od Katherine A. Rauen, William E. Tidyman

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A novel missense KIT mutation causing piebaldism in one Chinese family associated with café-au-lait macules and intertriginous freckling od Jia WX, Xiao XM, Wu JB, Ma YP, Ge YP, Li Q, Mao QX, Li CR

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Von Recklinghausen Neurofibromatosis od J Gordon Millichap

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Floret-like multinucleated giant cells in neurofibroma od Golka Dariusz, Shaktawat Sameer

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Neurofibromatosis, Down's syndrome, and acquired abnormalities od Syed Yousuf Ali, Vimala Manne, Ranjit Manne, Chennamaneni Himani

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