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NF1
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Neurofibromatosis von Recklinghausen type 1 (NF1) - clinical picture and molecular-genetics diagnostic
2015 |
First Faculty of Medicine, Second Faculty of Medicine
publication
Neurofibromatosis von Recklinghausen type I (NF1) - clinical picture in childhood, diagnosis and therapy
2023 |
Second Faculty of Medicine
publication
Neurofibromatosis
2011 |
Publication without faculty affiliation
publication
Neurofibromatosis von Recklinghausen type 1 (NF1) - the most common neurocutaneous disorder
2018 |
Second Faculty of Medicine
publication
Childhood overgrowth in patients with common NF1 microdeletions
2005 |
Second Faculty of Medicine
publication
Localized mosaic neurofibromatosis type 1
2022 |
Second Faculty of Medicine
publication
Novel mutations in the NF1 gene in Czech patients with neurofibromatosis type 1
2007 |
Second Faculty of Medicine
publication
Intragenic NF1 deletions in sinonasal mucosal malignant melanoma
2022 |
Faculty of Medicine in Hradec Králové
publication
Two independent chromosomal rearrangements, a very small (550 kb) duplication of the 7q subtelomeric region and an atypical 17q11.2 (NF1) microdeletion, in a girl with neurofibromatosis
2007 |
First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
publication
Idiopathic Aqueductal Stenosis and Developmental Speech Disorder in Children with Neurofibromatosis von Recklinghausen type 1-Two Case Reports
2012 |
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
Neurofibromatosis from the view of dermatologist
2015 |
Second Faculty of Medicine
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, Faculty of Physical Education and Sport, Second Faculty of Medicine
publication
Epigenetic profiling reveals a subset of pediatric-type glioneuronal tumors characterized by oncogenic gene fusions involving several targetable kinases
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
Primary cutanous desmoplastic melanoma with collagen rosettes and pseudoglandular features
2021 |
Faculty of Medicine in Pilsen
publication
Hereditary pheochromocytoma and paraganglioma
2012 |
First Faculty of Medicine
publication
S100 and CD34 positive spindle cell tumor with prominent perivascular hyalinization and a novel NCOA4-RET fusion
2019 |
Faculty of Medicine in Pilsen
publication
Neurofibromatosis von Recklinghausen
2009 |
Second Faculty of Medicine
publication
Monozygotic twins with Legius syndrome and differential diagnosis of Legius syndrome and neurof bromatosis type 1
2021 |
Second Faculty of Medicine
publication
Familial pulmonary fibrosis - guidelines for diagnostics and treatment
2020 |
Second Faculty of Medicine
publication
Hereditary pheochromocytoma and paraganglioma
2012 |
Second Faculty of Medicine, Central Library of Charles University
publication
Recommendations for Preventive Care for Women with Rare Genetic Cause of Breast and Ovarian Cancer
2019 |
First Faculty of Medicine
publication
Mutation analysis of Son of Sevenless in juvenile myelomonocytic leukemia
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
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
Gastrointestinal stromal tumor (GIST): advances in 2013
2014 |
Faculty of Medicine in Pilsen
publication
Molecular mechanisms of primary and secondary resistance, molecular-genetic features and characteristics of KIT/PDGFRA non-mutated GISTs
2017 |
Second Faculty of Medicine
publication
Neurofibromatosis von Recklinghausen type 1 - current knowledge
2004 |
Publication without faculty affiliation
publication
A girl with neurofibromatosis type 1, atypical autism and mosaic ring chromosome 17
2007 |
Second Faculty of Medicine