Results 81 to 90 of about 35,221 (221)

Triple-Layer Chess: An Analogy for Multi-Dimensional Health Policy Partnerships [PDF]

, 2007
The focus is the Jefferson County Access Program.

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Neuropathic Pain and Enlarged Nerves in Adult Noonan Syndrome and Noonan Syndrome With Multiple Lentigines: Health‐Related Quality of Life and Neurologic Symptoms

American Journal of Medical Genetics Part A, Volume 200, Issue 6, Page 1442-1451, June 2026.
ABSTRACT Noonan syndrome (NS) and the clinically related Noonan syndrome with multiple lentigines (NSML) belong to the group of RASopathies. Although pain is not mentioned as a characteristic feature, it has recently been reported as a clinically significant problem.
Jos M. T. Draaisma, Wesley Reintjes, Erika Leenders, Fieke Draaisma, Melanie Burgers, Lotte Kleimeier, Marco Tartaglia, Merel Klaassens, Ruud Becks, Steven Renes, Ellen Wingbermühle, Nicol C. Voermans, Nens van Alfen   +12 more
wiley   +1 more source

Constituent Mail Analysis Project (CMAP)

, 2003
As presented at IASSIST 2003 ...
Herndon, Joel, Nelson, Naomi
openaire   +1 more source

Anterior tibialis cmap amplitude correlations with impairment in CMT1A [PDF]

Muscle & Nerve, 2013
Introduction: CMT1A is the most common form of Charcot‐Marie‐Tooth disease (CMT), a slowly progressive neuropathy in which impairment is length dependent. Fibular nerve conduction studies to the anterior tibialis muscle (AT) may serve as a physiological marker of disease progression in patients with CMT1A.
Kelsey, Komyathy, Stephanie, Neal, Shawna, Feely, Lindsey J, Miller, Richard A, Lewis, George, Trigge, Carly E, Siskind, Michael E, Shy, Sindhu, Ramchandren   +8 more
openaire   +2 more sources

PACS2 Alleviates Sepsis‐Induced Myopathy by Activating ERK–MAPK Signalling Pathway to Suppress ER‐Phagy

Journal of Cachexia, Sarcopenia and Muscle, Volume 17, Issue 3, June 2026.
ABSTRACT Background Sepsis‐induced myopathy (SIM) is a common and life‐threatening complication, but its underlying mechanisms remain poorly understood. PACS2, a key resident protein at mitochondria‐associated endoplasmic reticulum membranes (MAMs), regulates ER homeostasis under various pathological conditions.
Xuexin Li, Zu‐an Shi, Fei He, Guo Mu, Feixiang Wang, Bowen Sun, Xiaobin Wang, Li Liu   +7 more
wiley   +1 more source

Transit-Oriented Development in the Chicago Region: Efficient and Resilient Communities for the 21st Century [PDF]

, 2013
In this report CNT researchers evaluated the dynamics of the Chicago Region's 367 fixed Metra and CTA rail stations and station areas between 2000 and 2010.

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Utility of Far‐Field Potentials as a Biomarker of Neurodegeneration in Spinal Muscular Atrophy

Muscle &Nerve, Volume 73, Issue 6, Page 1089-1095, June 2026.
ABSTRACT Introduction/Aims Far field potentials (FFP) have been proposed as a reliable neurophysiological prognostic biomarker in amyotrophic lateral sclerosis (ALS). This study evaluated the utility of ulnar nerve FFP as a robust research biomarker of lower motor neuron degeneration in spinal muscular atrophy (SMA).
Aicee Dawn Calma, Nathan Pavey, Cláudia Santos Silva, Yukiko Tsuji, Amirul Ab Ghapar, Katrina Morris, Matthew C. Kiernan, Michelle A. Farrar, Parvathi Menon, Steve Vucic   +9 more
wiley   +1 more source

The Diagnostic Potential of Axon Excitability Is Consistent Across Hand Muscles in Amyotrophic Lateral Sclerosis

Muscle &Nerve, Volume 73, Issue 6, Page 1138-1145, June 2026.
ABSTRACT Introduction/Aims Recent work suggests that nerve excitability testing has diagnostic potential in amyotrophic lateral sclerosis (ALS). The diagnostic performance of nerve excitability across hand muscles is currently unknown. This study aimed to assess if muscles of the so‐called split hand (abductor pollicis brevis [APB], first dorsal ...
Alana K. O. Hodgson, Christopher J. McDermott, Pamela J. Shaw, James J. P. Alix   +3 more
wiley   +1 more source

Current evidence for treatment with nusinersen for spinal muscular atrophy : a systematic review [PDF]

, 2019
Recent discovery of nusinersen, an antisense oligonucleotide drug, has provided encouragement for improving treatment of spinal muscular atrophy. No therapeutic options currently exist for this autosomal recessive motor neuron disorder.
Meylemans, Antoon, De Bleecker, Jan
core   +1 more source

Contemporary analysis of phrenic nerve injuries following cryoballoon-based pulmonary vein isolation: A single-centre experience with the systematic use of compound motor action potential monitoring.

PLoS ONE, 2020
BackgroundPhrenic nerve injury (PNI) remains one of the most frequent complications during cryoballoon-based pulmonary vein isolation (CB-PVI). Since its introduction in 2013, the use of compound motor action potential (CMAP) for the prevention of PNI ...
Omar Anwar, Melanie A Gunawardene, Jannis Dickow, Katharina Scherschel, Christiane Jungen, Paula Münkler, Christian Eickholt, Stephan Willems, Nele Gessler, Christian Meyer   +9 more
doaj   +1 more source