Background: Neurofibromatosis type I (NF1) is a rare genetic disorder, associated with some physical symptoms including spots and tiny bumps on the skin, and internal organ involvement. People suffering from neurofibromatosis face various challenges in their daily lives. However, there is little understanding on how patients deal with neurofibromatosis. This study aimed to investigate the life challenges of patients with NF1. Methods: This qualitative study was performed by implementing a grounded theory with the cooperation of the Society for Neurofibromatosis Patients over the course of 15 months in 2019 across 4 provinces in Iran. Twenty-four patients with NF1 were interviewed. An analysis was performed using the constant comparative met...
Background:. Neurofibromatosis Type 1 (NF1) is the most common type of neurogenetic disorder with a ...
Neurofibromatosis type 2 (Nf2) is an inherited autosomal dominant syndrome characterised by the deve...
Abstract Neurofibromatosis type 1 (NF1) is a genetic, autosomal dominant multi-organ disease charact...
Background: Neurofibromatosis Type 1 (NF1) is a common autosomal disorder; the criteria for the diag...
Context: Neurofibromatosis type 1 (NF1) is one of the most common genetic skin disorders that impose...
Objective: To explore the impact of plexiform neurofibromas on the lives of adults with neurofibroma...
Neurofibromatosis Type 1 (NF1, von Recklinghausen’s disease) is among the more common autosomal domi...
BACKGROUND: Patient engagement is increasingly recognized as a valuable, essential aspect of Neurofi...
Neurofibromatosis Type 1 (NF1) is a dominantly inherited disorder (births incidence: 1/3000) with a ...
Neurofibromatosis Type 1 (NF1) is a dominantly inherited disorder (births incidence: 1/3000) with a ...
International audienceABSTRACT: BACKGROUND: Neurofibromatosis 1 (NF-1), a common autosomal dominant ...
Background and purpose: Neurofibromatosis type 1 (NF1) is a dominant genetic disorder of the skin an...
Aims: To explore the day-to-day experience of young people living with neurofibromatosis type 1 in t...
The purpose of this timeline research project is to provide an outline of the discovery of Neurofibr...
There is a shortage of follow-up studies of Neurofibromatosis type 1 (NF1),an autosomal dominantly i...
Background:. Neurofibromatosis Type 1 (NF1) is the most common type of neurogenetic disorder with a ...
Neurofibromatosis type 2 (Nf2) is an inherited autosomal dominant syndrome characterised by the deve...
Abstract Neurofibromatosis type 1 (NF1) is a genetic, autosomal dominant multi-organ disease charact...
Background: Neurofibromatosis Type 1 (NF1) is a common autosomal disorder; the criteria for the diag...
Context: Neurofibromatosis type 1 (NF1) is one of the most common genetic skin disorders that impose...
Objective: To explore the impact of plexiform neurofibromas on the lives of adults with neurofibroma...
Neurofibromatosis Type 1 (NF1, von Recklinghausen’s disease) is among the more common autosomal domi...
BACKGROUND: Patient engagement is increasingly recognized as a valuable, essential aspect of Neurofi...
Neurofibromatosis Type 1 (NF1) is a dominantly inherited disorder (births incidence: 1/3000) with a ...
Neurofibromatosis Type 1 (NF1) is a dominantly inherited disorder (births incidence: 1/3000) with a ...
International audienceABSTRACT: BACKGROUND: Neurofibromatosis 1 (NF-1), a common autosomal dominant ...
Background and purpose: Neurofibromatosis type 1 (NF1) is a dominant genetic disorder of the skin an...
Aims: To explore the day-to-day experience of young people living with neurofibromatosis type 1 in t...
The purpose of this timeline research project is to provide an outline of the discovery of Neurofibr...
There is a shortage of follow-up studies of Neurofibromatosis type 1 (NF1),an autosomal dominantly i...
Background:. Neurofibromatosis Type 1 (NF1) is the most common type of neurogenetic disorder with a ...
Neurofibromatosis type 2 (Nf2) is an inherited autosomal dominant syndrome characterised by the deve...
Abstract Neurofibromatosis type 1 (NF1) is a genetic, autosomal dominant multi-organ disease charact...