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Guillain-Barré syndrome

Lancet, 2005-11, Vol.366 (9497), p.1653-1666

2005

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Guillain–Barré Syndrome Associated with Zika Virus Infection in Colombia

The New England journal of medicine, 2016-10, Vol.375 (16), p.1513-1523

2016

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Rhabdomyolysis: an evaluation of 475 hospitalized patients

Medicine (Baltimore), 2005-11, Vol.84 (6), p.377-385

2005

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A Dominant Mutation in FBXO38 Causes Distal Spinal Muscular Atrophy with Calf Predominance

American journal of human genetics, 2013-11, Vol.93 (5), p.976-983

2013

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Original research: Second IVIg course in Guillain-Barré syndrome with poor prognosis: the non-randomised ISID study

Journal of neurology, neurosurgery and psychiatry, 2020-02, Vol.91 (2), p.113-121

2020

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Prospective Evaluation of Health Care Provider and Patient Assessments in Chemotherapy-Induced Peripheral Neurotoxicity

Neurology, 2021-08, Vol.97 (7), p.e660

2021

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Subcutaneous immunoglobulin for maintenance treatment in chronic inflammatory demyelinating polyneuropathy (The PATH Study): study protocol for a randomized controlled trial

Trials, 2016-07, Vol.17 (1), p.345-345, Article 345

2016

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Pharmacometric analysis linking immunoglobulin exposure to clinical efficacy outcomes in chronic inflammatory demyelinating polyneuropathy

CPT: pharmacometrics and systems pharmacology, 2021-08, Vol.10 (8), p.839-850

2021

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Neuropathological alterations in diabetic truncal neuropathy: evaluation by skin biopsy

Journal of neurology, neurosurgery and psychiatry, 1998-11, Vol.65 (5), p.762-766

1998

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Changing outcome in inflammatory neuropathies: Rasch-comparative responsiveness

Neurology, 2014-12, Vol.83 (23), p.2124-2132

2014

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Perioperative bilateral median neuropathy

Anesthesiology (Philadelphia), 2002-12, Vol.97 (6), p.1632-1634

2002

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Autonomic and peripheral (sensorimotor) neuropathy in chronic liver disease: A clinical and electrophysiologic study

Hepatology (Baltimore, Md.), 1999-06, Vol.29 (6), p.1698-1703

1999

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Congenital End-Plate Acetylcholinesterase Deficiency Caused by a Nonsense Mutation and an A→G Splice-Donor–Site Mutation at Position +3 of the Collagenlike-Tail–Subunit Gene ( COLQ): How Does G at Position +3 Result in Aberrant Splicing?

American journal of human genetics, 1999-09, Vol.65 (3), p.635-644

1999

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Epidermal nerve fiber density: normative reference range and diagnostic efficiency

Archives of neurology (Chicago), 1998-12, Vol.55 (12), p.1513

1998

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Intravenous immunoglobulin treatment for mild Guillain-Barré syndrome: an international observational study

Journal of neurology, neurosurgery and psychiatry, 2021-10, Vol.92 (10), p.1080-1088

2021

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Clinical and genetic description of a family with Charcot-Marie-Tooth disease type 1B from a transmembrane MPZ mutation

Muscle & nerve, 2004-06, Vol.29 (6), p.867-869

2004

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Maintenance of the long-term effectiveness of tramadol in treatment of the pain of diabetic neuropathy

Journal of diabetes and its complications, 2000-03, Vol.14 (2), p.65-70

2000

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Phase I and pharmacologic study of paclitaxel and cisplatin with granulocyte colony-stimulating factor: neuromuscular toxicity is dose-limiting

Journal of clinical oncology, 1993-10, Vol.11 (10), p.2010-2020

1993

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Assessment of thoracic paraspinal muscles in the diagnosis of ALS

Muscle & nerve, 1988-05, Vol.11 (5), p.484-492

1988

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Sequences of taxol and cisplatin: a phase I and pharmacologic study

Journal of clinical oncology, 1991-09, Vol.9 (9), p.1692-1703

1991

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Treatment of chronic inflammatory demyelinating polyneuropathy with cyclosporin-A

Journal of neurology, neurosurgery and psychiatry, 1996-02, Vol.60 (2), p.185-187

1996

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Effect of MRI on treatment results or decision making in patients with lumbosacral radiculopathy referred for epidural steroid injections: a multicenter, randomized controlled trial

Archives of internal medicine (1960), 2012-01, Vol.172 (2), p.134

2012

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Characterization of cDNA and genomic DNA encoding SERCA1, the Ca(2+)-ATPase of human fast-twitch skeletal muscle sarcoplasmic reticulum, and its elimination as a candidate gene for Brody disease

Genomics (San Diego, Calif.), 1995-12, Vol.30 (3), p.415-424

1995

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Molecular insight into the asymmetric distribution of pathogenetic human mitochondrial DNA deletions

Biochemical and biophysical research communications, 1991-01, Vol.174 (1), p.244-250

1991

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Visual Function 15 Years after Optic Neuritis : A Final Follow-up Report from the Optic Neuritis Treatment Trial

Ophthalmology (Rochester, Minn.), 2008-06, Vol.115 (6), p.1079-1082

Optic Neuritis Study Group

2008

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Guillain-Barré syndrome

Guillain–Barré Syndrome Associated with Zika Virus Infection in Colombia

Rhabdomyolysis: an evaluation of 475 hospitalized patients

A Dominant Mutation in FBXO38 Causes Distal Spinal Muscular Atrophy with Calf Predominance

Original research: Second IVIg course in Guillain-Barré syndrome with poor prognosis: the non-randomised ISID study

Prospective Evaluation of Health Care Provider and Patient Assessments in Chemotherapy-Induced Peripheral Neurotoxicity

Subcutaneous immunoglobulin for maintenance treatment in chronic inflammatory demyelinating polyneuropathy (The PATH Study): study protocol for a randomized controlled trial

Pharmacometric analysis linking immunoglobulin exposure to clinical efficacy outcomes in chronic inflammatory demyelinating polyneuropathy

Neuropathological alterations in diabetic truncal neuropathy: evaluation by skin biopsy

Changing outcome in inflammatory neuropathies: Rasch-comparative responsiveness

Perioperative bilateral median neuropathy

Autonomic and peripheral (sensorimotor) neuropathy in chronic liver disease: A clinical and electrophysiologic study

Congenital End-Plate Acetylcholinesterase Deficiency Caused by a Nonsense Mutation and an A→G Splice-Donor–Site Mutation at Position +3 of the Collagenlike-Tail–Subunit Gene ( COLQ): How Does G at Position +3 Result in Aberrant Splicing?

Epidermal nerve fiber density: normative reference range and diagnostic efficiency

Intravenous immunoglobulin treatment for mild Guillain-Barré syndrome: an international observational study

Clinical and genetic description of a family with Charcot-Marie-Tooth disease type 1B from a transmembrane MPZ mutation

Maintenance of the long-term effectiveness of tramadol in treatment of the pain of diabetic neuropathy

Phase I and pharmacologic study of paclitaxel and cisplatin with granulocyte colony-stimulating factor: neuromuscular toxicity is dose-limiting

Assessment of thoracic paraspinal muscles in the diagnosis of ALS

Sequences of taxol and cisplatin: a phase I and pharmacologic study

Treatment of chronic inflammatory demyelinating polyneuropathy with cyclosporin-A

Effect of MRI on treatment results or decision making in patients with lumbosacral radiculopathy referred for epidural steroid injections: a multicenter, randomized controlled trial

Characterization of cDNA and genomic DNA encoding SERCA1, the Ca(2+)-ATPase of human fast-twitch skeletal muscle sarcoplasmic reticulum, and its elimination as a candidate gene for Brody disease

Molecular insight into the asymmetric distribution of pathogenetic human mitochondrial DNA deletions

Visual Function 15 Years after Optic Neuritis : A Final Follow-up Report from the Optic Neuritis Treatment Trial

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