Citations 185

Hydrocephalus in neuromyelitis optica

Neurology | April 24, 2014 | Volume: 82 | Issue: 20 | Pages: 1841-1843

10.1212/wnl.0000000000000428 | PMID 24759842

Paraneoplastic Neuromyelitis Optica Spectrum Disorder Associated With Metastatic Carcinoid Expressing Aquaporin-4

JAMA Neurology | April 14, 2014 | Volume: 71 | Issue: 4 | Pages: 495

10.1001/jamaneurol.2013.6331 | PMID 24733266

Utility of an immunotherapy trial in evaluating patients with presumed autoimmune epilepsy

Neurology | April 4, 2014 | Volume: 82 | Issue: 18 | Pages: 1578-1586

10.1212/wnl.0000000000000383 | PMID 24706013

Purkinje Cell Cytoplasmic Antibody Type 1 (Anti-Yo) Autoimmunity in a Child With Down Syndrome

JAMA Neurology | January 14, 2014 | Volume: 71 | Issue: 3 | Pages: 347

10.1001/jamaneurol.2013.4551 | PMID 24424854

Rare combination of myasthenia and motor neuronopathy, responsive to Msc‐Ntf stem cell therapy

Muscle & Nerve | December 11, 2013 | Volume: 49 | Issue: 3 | Pages: 455-457

10.1002/mus.24143 | PMID 24327321

Asymptomatic lambert–eaton syndrome

Muscle & Nerve | November 21, 2013 | Volume: 49 | Issue: 5 | Pages: 764-767

10.1002/mus.24126 | PMID 24259319

ABSTRACTIntroductionAll descriptions of the Lambert–Eaton syndrome are based on symptomatic patients. We incidentally encountered electromyographic evidence of this syndrome in a patient being studied for another reason. The patient had controlled hypothyroidism and smoked for 9 pack‐years but never had symptoms of weakness or had evidence of cancer. Methods: Detailed electrophysiological and serological evaluations were undertaken in this study. Results: Neuromuscular transmission tests were consistent with a presynaptic disorder. Autoantibodies specific for P/Q‐type voltage‐gated calcium channels (VGCC) were detected in the serum and persisted throughout 7 years of follow‐up. Multiple IgG markers of thyrogastric autoimmunity also were detected. Conclusions: This demonstration of asymptomatic Lambert–Eaton syndrome persisting for 8 years provided novel insight into the natural history of the disorder. It is plausible that patients with a subclinical syndrome would have abrupt neuromuscular decompensation when challenged with medications that compromise the safety factor for synaptic transmission. Muscle Nerve 49: 764–767, 2014
Aquaporin 4 IgG Serostatus and Outcome in Recurrent Longitudinally Extensive Transverse Myelitis

JAMA Neurology | November 18, 2013 | Volume: 71 | Issue: 1 | Pages: 48

10.1001/jamaneurol.2013.5055 | PMID 24248262

Childhood Onset of Stiff-Man Syndrome

JAMA Neurology | October 7, 2013 | Volume: 70 | Issue: 12 | Pages: 1531

10.1001/jamaneurol.2013.4442 | PMID 24100349

Updated estimate of AQP4-IgG serostatus and disability outcome in neuromyelitis optica

Neurology | August 30, 2013 | Volume: 81 | Issue: 14 | Pages: 1197-1204

10.1212/wnl.0b013e3182a6cb5c | PMID 23997151

Activation of muscarinic acetylcholine receptors inhibits cell cycle progression of small cell lung carcinoma.

Cell Regulation | August 16, 2013 | Volume: 2 | Issue: 5 | Pages: 373-381

10.1091/mbc.2.5.373 | PMID 1654127

We previously reported that activation of muscarinic acetylcholine receptors (mAChR) of M3 subtype causes hydrolysis of phosphoinositides and inhibits voltage-gated Ca2+ channel activity in small cell lung carcinoma (SCLC) cells. We now report that mAChR activation causes exponentially growing SCLC cells to arrest in S and G2/M phases of the cell cycle, concomitant with a decrease in DNA synthesis. Cell cycle progression and DNA synthesis resume when mAChR are down-regulated. In serum-starved SCLC cells, mAChR activation inhibits DNA synthesis induced by serum, bombesin, insulin, or insulin-like growth factor-I. The finding that DNA synthesis is inhibited even when mAChR are activated after exposure of cells to growth factors indicates that decreased signal transduction by growth factor receptors is not the mechanism of mAChR-mediated growth inhibition. Our data suggest that mAChR activation disrupts a common event that is induced by different growth factors and is fundamental for cell cycle progression.