Multifocal nerve lesions andLZTR1germline mutations in segmental schwannomatosis

Mosaic Neurocutaneous Disorders and Their Causes

(2015) Martino Ruggieri et al.   Seminars in Pediatric Neurology

Whole exome sequencing reveals that the majority of schwannomatosis cases remain unexplained after excluding SMARCB1 and LZTR1 germline variants

(2014) Sonja Hutter et al.   ACTA NEUROPATHOLOGICA

Peripheral nerves and plexus

(2014) Mirko Pham et al.   CURRENT OPINION IN NEUROLOGY

Anterior interosseous nerve syndrome: Fascicular motor lesions of median nerve trunk

(2014) M. Pham et al.   NEUROLOGY

Mutations in LZTR1 add to the complex heterogeneity of schwannomatosis

(2014) M. J. Smith et al.   NEUROLOGY

Update from the 2011 International Schwannomatosis Workshop: From genetics to diagnostic criteria

(2013) Scott R. Plotkin et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas

(2013) Arkadiusz Piotrowski et al.   NATURE GENETICS

Accumulation of non-compressive fascicular lesions underlies NF2 polyneuropathy

(2012) P. Bäumer et al.   JOURNAL OF NEUROLOGY

Frequency of SMARCB1 mutations in familial and sporadic schwannomatosis

(2012) Miriam J. Smith et al.   NEUROGENETICS

Clinical Features of Schwannomatosis: A Retrospective Analysis of 87 Patients

(2012) V. L. Merker et al.   ONCOLOGIST

SMARCB1/INI1maternal germ line mosaicism in schwannomatosis

(2009) TJM Hulsebos et al.   CLINICAL GENETICS

Assessment of benign tumor burden by whole-body MRI in patients with neurofibromatosis 1

(2008) Victor-F. Mautner et al.   NEURO-ONCOLOGY