Latest papers

The Neurofibromatoses. Part 1: NF1.

Neurofibromatosis: advances in molecular genetics, diagnosis, and treatment. Introduction.

Neurofibromatosis presenting as generalized nerve thickening.

Treatment for genetic diseases.

Nf1 mutation expands an EGFR-dependent peripheral nerve progenitor that confers neurofibroma tumorigenic potential.

Giant Chiari network mimics intracardiac tumor in a case of neurofibramatosis

Isolated intestinal neurofibromatous proliferations in the absence of associated systemic syndromes.

Face transplant graft procurement: a preclinical and clinical study.

Multiple huge epidermal inclusion cysts mistaken as neurofibromatosis.

A child with intra-orbital oculomotor nerve schwannoma without neurofibromatosis.

JAMA patient page. Neurofibromatosis.

Zebrafish with mutations in mismatch repair genes develop neurofibromas and other tumors.

Photoclinic: moyamoya disease associated with neurofibromatosis 1.

Segmental neurofibromatosis associated with renal angiomyolipomas.

Large dorsal intercostal perforator flap in extensive neurofibromatosis.

Giant plexiform neurofibroma and suboccipital meningocele manifesting as segmental neurofibromatosis.

[Use of a vascularized fibula for spinal reconstruction in neurofibromatosis]

Cystoperitoneal shunt as alternative treatment for a giant thoracic meningocele in a patient with neurofibromatosis.

Life-threatening subcutaneous hematoma

Leukemia-associated NF1 inactivation in patients with pediatric T-ALL and AML lacking evidence for neurofibromatosis.