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Search for publications relevant for "neurofibromatosis type 1"
neurofibromatosis type 1
Publication
Class
Person
Publication
Programmes
publication
Novel mutations in the NF1 gene in Czech patients with neurofibromatosis type 1
2007 |
Second Faculty of Medicine
publication
Serious vasculopathies in neurofibromatosis type 1
2019 |
Faculty of Medicine in Hradec Králové
publication
Localized mosaic neurofibromatosis type 1
2022 |
Second Faculty of Medicine
publication
The importance of advanced parental age in the origin of neurofibromatosis type 1
2012 |
Second Faculty of Medicine
publication
Massive intramuscular bleeding in a neurofibromatosis type 1 patient
2018 |
Publication without faculty affiliation
publication
A girl with neurofibromatosis type 1, atypical autism and mosaic ring chromosome 17
2007 |
Second Faculty of Medicine
publication
Brain gliomas, hydrocephalus and idiopathic aqueduct stenosis in children with neurofibromatosis type 1
2019 |
Second Faculty of Medicine
publication
Anti-vimentin antibodies and neuron-specific enolase in children with neurofibromatosis type-1
2007 |
Second Faculty of Medicine
publication
Gynecomastia with pseudoangiomatous stromal hyperplasia and multinucleated giant cells. Association with neurofibromatosis type 1
2002 |
Faculty of Medicine in Pilsen
publication
Comment on sudden death due to rupture of the right internal carotid artery in neurofibromatosis type 1 by Liang et al
2016 |
Faculty of Medicine in Hradec Králové
publication
Mitotic recombination and compound-heterozygous mutations are predominant NF1-inactivating mechanisms in children with juvenile myelomonocytic leukemia and neurofibromatosis type 1
2010 |
Second Faculty of Medicine
publication
Multinucleated floret-like giant cells in sporadic and NF1-associated neurofibromas: a clinicopathologic study of 94 cases
2010 |
Central Library of Charles University
publication
Neurofibromatosis von Recklinghausen type I (NF1) - clinical picture in childhood, diagnosis and therapy
2023 |
Second Faculty of Medicine
publication
Biallelic inactivation of the NF1 tumour suppressor gene in juvenile myelomonocytic leukaemia: Genetic evidence of driver function and implications for diagnostic workup
2024 |
Second Faculty of Medicine
publication
Hybrid peripheral nerve sheath tumors, including a malignant variant in type 1 neurofibromatosis
2013 |
Faculty of Medicine in Pilsen
publication
Mid-aortic syndrome with renovascular hypertension and multisystem involvement in a girl with familiar neurofibromatosis von Recklinghausen type 1
2007 |
First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
publication
Neurofibromatosis
2011 |
Publication without faculty affiliation
publication
Malignant Peripheral Nerve Sheath Tumor - Two Case Reports
2009 |
First Faculty of Medicine
publication
Hereditary pheochromocytoma and paraganglioma
2012 |
First Faculty of Medicine
publication
Malignant schwannoma - a difficult journey to final diagnosis
2015 |
First Faculty of Medicine
publication
A composite neoplastic lesion of the vulva with mixed features of fibroadenoma and hidradenoma papilliferum combined with pseudoangiomatous stromal hyperplasia containing multinucleated giant cells
2014 |
Faculty of Medicine in Pilsen
publication
Monozygotic twins with Legius syndrome and differential diagnosis of Legius syndrome and neurof bromatosis type 1
2021 |
Second Faculty of Medicine
publication
Childhood overgrowth in patients with common NF1 microdeletions
2005 |
Second Faculty of Medicine
publication
Pheochromocytoma
2009 |
First Faculty of Medicine
publication
Pheochromocytoma - clinical aspects
2009 |
First Faculty of Medicine
publication
Functional Repair Assay for the Diagnosis of Constitutional Mismatch Repair Deficiency From Non-Neoplastic Tissue
2019 |
Second Faculty of Medicine
publication
Mutation analysis of Son of Sevenless in juvenile myelomonocytic leukemia
2007 |
Second Faculty of Medicine
publication
Hereditary pheochromocytoma and paraganglioma
2012 |
Central Library of Charles University, Second Faculty of Medicine
publication
Germline CBL mutations cause developmental abnormalities and predispose to juvenile myelomonocytic leukemia
2010 |
Second Faculty of Medicine
publication
Neurofibromatosis from the view of dermatologist
2015 |
Second Faculty of Medicine