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Literature DB >> 1289736

Nerve root and sciatic trunk enlargement in Déjérine-Sottas disease: MRI appearances.

N Masuda¹, H Hayashi, H Tanabe.

Abstract

Entities: Disease

Mesh：

Year: 1992 PMID： 1289736 DOI： 10.1007/bf00588275

Source DB: PubMed Journal: Neuroradiology ISSN： 0028-3940 Impact factor: 2.804

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5 in total

1. [On hypertrophic neuritis (Roussy-Cornil)].

Authors: G BRUNS
Journal: Beitr Pathol Anat Date: 1951

2. Genetic linkage of hereditary motor and sensory neuropathy type I (Charcot-Marie-Tooth disease) to markers of chromosomes 1 and 17.

Authors: J C Defesche; J E Hoogendijk; M de Visser; O de Visser; P A Bolhuis
Journal: Neurology Date: 1990-09 Impact factor: 9.910

3. Neurofibromatous neuropathy.

Authors: P K Thomas; R H King; T R Chiang; F Scaravilli; A K Sharma; A W Downie
Journal: Muscle Nerve Date: 1990-02 Impact factor: 3.217

4. Gene for von Recklinghausen neurofibromatosis is in the pericentromeric region of chromosome 17.

Authors: D Barker; E Wright; K Nguyen; L Cannon; P Fain; D Goldgar; D T Bishop; J Carey; B Baty; J Kivlin
Journal: Science Date: 1987-05-29 Impact factor: 47.728

5. Neurofibromatosis, Charcot-Marie-Tooth disease, or both?

Authors: K L Roos; R M Pascuzzi; D W Dunn
Journal: Neurofibromatosis Date: 1989

5 in total

6 in total

Review 1. Plexopathy.

Authors: B C Bowen; D J Seidenwurm
Journal: AJNR Am J Neuroradiol Date: 2008-02 Impact factor: 3.825

Nerve root and sciatic trunk enlargement in Déjérine-Sottas disease: MRI appearances.

1. [On hypertrophic neuritis (Roussy-Cornil)].

2. Genetic linkage of hereditary motor and sensory neuropathy type I (Charcot-Marie-Tooth disease) to markers of chromosomes 1 and 17.

3. Neurofibromatous neuropathy.

4. Gene for von Recklinghausen neurofibromatosis is in the pericentromeric region of chromosome 17.

5. Neurofibromatosis, Charcot-Marie-Tooth disease, or both?

Review 1. Plexopathy.

2. MRI of enlarged dorsal ganglia, lumbar nerve roots, and cranial nerves in polyradiculoneuropathies.

3. MR imaging of the spine in epidermal nevus syndrome.

4. MR imaging of the cauda equina in hereditary motor sensory neuropathies: correlations with sural nerve biopsy.

5. MRI of peripheral nerves and pathology of sural nerves in hereditary motor and sensory neuropathy type III.

6. PTPN11 mutation manifesting as LEOPARD syndrome associated with hypertrophic plexi and neuropathic pain.