نتایج جستجو برای: muscle paralysis

تعداد نتایج: 344804  

2013
Kofi Boahene

Facial animation is an essential part of human communication and one of the main means of expressing emotions, indexing our physiologic state and providing nonverbal cues. The loss of this important human quality due to facial paralysis can be devastating and is often associated with depression, social isolation and poor quality of life. Interruption of the neuromuscular pathway from the facial...

2011
Abbi Lulsegged Christina Wlodek Michela Rossi

Objectives. To describe 2 cases of thyrotoxic periodic paralysis. Methods. We report of 2 cases of thyrotoxic periodic paralysis in 2 individuals from 2 different backgrounds with emphasis on their presentation and treatment. We also conducted a literature search to put together an update review of thyrotoxic periodic paralysis. Results. A 47-year-old Chinese and 28-year-old Caucasian male pres...

2012
Manoj K. Mittal Alejandro A. Rabinstein

Chondrocalcinosis associated with Gitelman syndrome (GS) presents in young adults with either no symptoms or joint pain, muscle weakness, muscle cramps, paresthesias, episodes of tetany, or hypokalemic paralysis. Spinal cord meningiomas present with gradual onset of lower extremities weakness, numbness, pain, or balance problem. We report a 76 year old gentleman who presented with gradually pro...

Journal: :Acta orthopaedica Belgica 2004
Ilse Degreef Luc De Smet

A case of an older female patient with paralysis of the anterior interosseous nerve is reported. During exploration an accessory muscle slip running from the coronoid process of the ulna towards the flexor pollicis longus (Gantzer's muscle) was found compressing the nerve.

Journal: :The Turkish journal of pediatrics 2010
Faruk Incecik Mihriban Ozlem Hergüner Sakir Altunbaşak Frank Lehman-Horn

Hypokalemic periodic paralysis (HypoPP) is an autosomal dominant disorder characterized by episodic attacks of muscle weakness associated with a decrease in blood potassium levels. Recently, mutations in the gene coding for the skeletal muscle voltage-gated sodium channel alpha subunit (SCN4A) have been reported. We detected the R672H mutation in one HypoPP Turkish family.

2017
Miyuki Niki Taihei Tachikawa Yuka Sano Hiroki Miyawaki Aisa Matoi Yukari Okano Nobutaka Kariya Tsuneo Tatara Munetaka Hirose

BACKGROUND Preoperative vocal cord paralysis is a risk factor for postoperative respiratory distress following extubation after general anesthesia. We present an unusual case where a geriatric patient developed airway obstruction after robot-assisted laparoscopic prostatectomy. CASE PRESENTATION A 67-year-old male, who had suffered from left vocal cord paralysis of unknown etiology, was sched...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2000
R L Ruff

H periodic paralysis (HypoPP), described a recent issue of PNAS by Jurkat-Rott and colleagues (1), has great scientific and clinical interest because its pathophysiology touches on several important properties of skeletal muscle. Besides providing the force for movement, skeletal muscle is an electrically excitable tissue and an important endocrine target organ as the largest protein store for ...

2014
André Auersvald Luiz A. Auersvald

SUMMARY Adequate neck contour is one of the goals in facial rejuvenation. In some patients, treating the submandibular salivary gland (SMSG) ensures a satisfying result. Hematoma, sialoma, and paralysis of the depressors of the lower lip may occur when the deep neck is approached. The objective of this work is to present a new tactic to prevent the aforementioned complications. Two hundred fort...

Journal: :The Journal of Cell Biology 2001
Carmen Cifuentes-Diaz Tony Frugier Francesco D. Tiziano Emmanuelle Lacène Natacha Roblot Vandana Joshi Marie Helene Moreau Judith Melki

Spinal muscular atrophy (SMA) is characterized by degeneration of motor neurons of the spinal cord associated with muscle paralysis and caused by mutations of the survival motor neuron gene (SMN). To determine whether SMN gene defect in skeletal muscle might have a role in SMA pathogenesis, deletion of murine SMN exon 7, the most frequent mutation found in SMA, has been restricted to skeletal m...

2010
Vishantie Dostal Christopher D. Link

Accumulation of the β-amyloid peptide (Aβ) is generally believed to be central to the induction of Alzheimer's disease, but the relevant mechanism(s) of toxicity are still unclear. Aβ is also deposited intramuscularly in Inclusion Body Myositis, a severe human myopathy. The intensely studied nematode worm Caenorhabditis elegans can be transgenically engineered to express human Aβ. Depending on ...

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