Neurofibromatosis type 1 is a multisystemic disease. It may manifest as abnormalities of the nervous tissue, bones, soft tissue, or skin. Autoimmune disease associated with NF1 can be seen. Diabetes mellitus is rarely seen in association with NF1. Here, we report a case with established NF1 who also had a diagnosis of diabetes mellitus. © 2013 Bayram Ozhan et al
Neurofibromatosis type 1 (NF1) is one of the most frequent genetic disorders, affecting 1:3,000 worl...
Neurofibromatosis type 1 (NF-1) is a common hereditary neurocutaneous disease, with known gene mutat...
INTRODUCTION: Neurofibromatosis type 1 (NF1) or Von Reckligausen disease is characterized by multipl...
Neurofibromatosis type 1 is a multisystemic disease. It may manifest as abnormalities of the nervous...
Neurofibromatosis type 1 is a multisystemic disease. It may manifest as abnormalities of the nervous...
Introduction: Endocrine disorders during Von Recklinghausen’s Disease or neurofibromatosis type 1 ...
BACKGROUND: The hereditary predisposition to diabetes is only partially explained by genes identifie...
Neurofibromatosis type I (NF1) is an autosomal dominant disorder with involvement of both the cutane...
BACKGROUND: Neurofibromatosis type 1 (NF1) is a multisystemic disorder with genetic background, char...
Abstract: 1Neurofibromatosis (NF) is a group of genetic disorders: NF1, NF2 and schwannomatosis (shw...
The association of Neurofibromatosis 1 (NF 1), an autosomal dominant genetic disease with autoimmune...
Neurofibromatosis type 1 (NF1) is one of the most frequent genetic disorders, affecting 1:3,000 worl...
Introduction - Neurofibromatosis type 1 (NF1), known as von Recklinghausen’s disease, is characteri...
Neurofibromatosis type 1 (NF-1) is a significant autosomal dominant disorder with a wide spectrum of...
Neurofibromatosis type 1 (NF1) or Von Recklinghausen's disease is a dominantly inherited genetic, mu...
Neurofibromatosis type 1 (NF1) is one of the most frequent genetic disorders, affecting 1:3,000 worl...
Neurofibromatosis type 1 (NF-1) is a common hereditary neurocutaneous disease, with known gene mutat...
INTRODUCTION: Neurofibromatosis type 1 (NF1) or Von Reckligausen disease is characterized by multipl...
Neurofibromatosis type 1 is a multisystemic disease. It may manifest as abnormalities of the nervous...
Neurofibromatosis type 1 is a multisystemic disease. It may manifest as abnormalities of the nervous...
Introduction: Endocrine disorders during Von Recklinghausen’s Disease or neurofibromatosis type 1 ...
BACKGROUND: The hereditary predisposition to diabetes is only partially explained by genes identifie...
Neurofibromatosis type I (NF1) is an autosomal dominant disorder with involvement of both the cutane...
BACKGROUND: Neurofibromatosis type 1 (NF1) is a multisystemic disorder with genetic background, char...
Abstract: 1Neurofibromatosis (NF) is a group of genetic disorders: NF1, NF2 and schwannomatosis (shw...
The association of Neurofibromatosis 1 (NF 1), an autosomal dominant genetic disease with autoimmune...
Neurofibromatosis type 1 (NF1) is one of the most frequent genetic disorders, affecting 1:3,000 worl...
Introduction - Neurofibromatosis type 1 (NF1), known as von Recklinghausen’s disease, is characteri...
Neurofibromatosis type 1 (NF-1) is a significant autosomal dominant disorder with a wide spectrum of...
Neurofibromatosis type 1 (NF1) or Von Recklinghausen's disease is a dominantly inherited genetic, mu...
Neurofibromatosis type 1 (NF1) is one of the most frequent genetic disorders, affecting 1:3,000 worl...
Neurofibromatosis type 1 (NF-1) is a common hereditary neurocutaneous disease, with known gene mutat...
INTRODUCTION: Neurofibromatosis type 1 (NF1) or Von Reckligausen disease is characterized by multipl...