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Search for publications relevant for "NF1 gene"
NF1 gene
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
Idiopathic Aqueductal Stenosis and Developmental Speech Disorder in Children with Neurofibromatosis von Recklinghausen type 1-Two Case Reports
2012 |
Second Faculty of Medicine
publication
Localized mosaic neurofibromatosis type 1
2022 |
Second Faculty of Medicine
publication
Neurofibromatosis
2011 |
Publication without faculty affiliation
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
S100 and CD34 positive spindle cell tumor with prominent perivascular hyalinization and a novel NCOA4-RET fusion
2019 |
Faculty of Medicine in Pilsen
publication
The importance of advanced parental age in the origin of neurofibromatosis type 1
2012 |
Second Faculty of Medicine
publication
Hereditary pheochromocytoma and paraganglioma
2012 |
First 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
Hereditary pheochromocytoma and paraganglioma
2012 |
Second Faculty of Medicine, 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
A girl with neurofibromatosis type 1, atypical autism and mosaic ring chromosome 17
2007 |
Second Faculty of Medicine
publication
Neurofibromatosis von Recklinghausen type 1 (NF1) - clinical picture and molecular-genetics diagnostic
2015 |
First Faculty of Medicine, Second Faculty of Medicine
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
Molecular mechanisms of primary and secondary resistance, molecular-genetic features and characteristics of KIT/PDGFRA non-mutated GISTs
2017 |
Second Faculty of Medicine
publication
Gastrointestinal stromal tumors - Summary of mutational status of the primary/secondary KIT/PDGFRA mutations, BRAF mutations and SDH defects
2019 |
Second Faculty of Medicine, Central Library of Charles University