Results 171 to 180 of about 47,993 (230)

Ccl5 establishes an autocrine high-grade glioma growth regulatory circuit critical for mesenchymal glioblastoma survival [PDF]

, 2017
Gutmann, David H, Hambardzumyan, Dolores, Ma, Yu, Pan, Yuan, Smithson, Laura J   +4 more
core   +2 more sources

Neurofibromatosis Type 2: A Rare Case of Multiple Intracranial Schwannomas, Meningiomas, and Ependymomas (MISME) Syndrome and Literature Review. [PDF]

Cureus
Hamza L, Yahya N, Wafa H, Loubna C, Sara L, Nawal A.   +5 more
europepmc   +1 more source

Subacute brainstem ischemic syndrome in juvenile neurofibromatosis type 2: An underrecognized condition. [PDF]

Clin Case Rep, 2022
Blauen A, Lenfant C, Duprez T, Nassogne MC.   +3 more
europepmc   +1 more source

Management Strategies of Neurofibromatosis Type 2 in Pediatric Patients : Challenges and Emerging Therapies. [PDF]

J Korean Neurosurg Soc
Lee JS.
europepmc   +1 more source

Efficacy of Combined Dabrafenib and Trametinib Therapy in BRAFV600E Mutant Intrahepatic Cholangiocarcinoma with a Neurofibromatosis Type 2 Mutation. [PDF]

Intern Med
Yoshida J, Sugiyama K, Owaki S, Ito T, Yamaguchi Y, Emi R, Sako Y, Satoh M, Ino R, Kato K, Shiraishi K, Shimada M, Hattori H, Kitagawa C.   +13 more
europepmc   +1 more source

Bevacizumab for Vestibular Schwannomas in Neurofibromatosis Type 2: A Systematic Review of Tumor Control and Hearing Preservation. [PDF]

J Clin Med
Screnci M, Puechmaille M, Berton Q, Khalil T, Mom T, Coll G.   +5 more
europepmc   +1 more source

KIR2DL5 mutation and loss underlies sporadic dermal neurofibroma pathogenesis and growth [PDF]

, 2017
Anastasaki, Corina, Dahiya, Sonika, Gutmann, David H   +2 more
core   +3 more sources

Erratum: Gene replacement therapy in a schwannoma mouse model of neurofibromatosis type 2. [PDF]

Mol Ther Methods Clin Dev
Prabhakar S, Beauchamp RL, Cheah PS, Yoshinaga A, Abou Haidar E, Lule S, Mani G, Maalouf K, Stemmer-Rachamimov A, Jung DH, Welling DB, Giovannini M, Plotkin SR, Maguire CA, Ramesh V, Breakefield XO.   +15 more
europepmc   +1 more source

Oncogenetic testing, diagnosis and follow-up in Birt-Hogg-Dubé syndrome, familial atypical multiple mole melanoma syndrome and neurofibromatosis 1 and 2 [PDF]

, 2015
't Kint de Roodenbeke, Daphné, Baurain, Jean-François, Brochez, Lieve, Caplanusi, Teofila, Claes, Kathleen, Hulstaert, Frank, Legius, Eric, Poppe, Bruce, Robays, Jo, Rottey, Sylvie, Schrijvers, Dirk, Stordeur, Sabine, Ullman, Urielle, Van Maerken, Tom   +13 more
core  

Neurofibromatosis Type 2 Presenting as Symptomatic Gallbladder Hydrops: A Rare Case Report and Literature Review. [PDF]

Case Rep Pediatr
Hafez B, Alwan JS, El Hout W, Koussa K, El Annan T, Noun D, Zaghal A.   +6 more
europepmc   +1 more source