Results 81 to 90 of about 62,561 (290)

Spasticity in children [PDF]

, 2012
Spasticity is a wide spectrum disease that affects all age groups. Spasticity in children may have diverse etiologies; this article will focus on children with spasticity, most of whom have diagnoses of cerebral palsy; as approximately two thirds of all ...
Awaad, Yasser, Rizk, Tamer
core   +1 more source

sj-pdf-3-jhs-10.1177_17531934231192843 - Supplemental material for Expert consensus on the surgical evaluation and management of upper extremity spasticity in adults

, 2023
Supplemental material, sj-pdf-3-jhs-10.1177_17531934231192843 for Expert consensus on the surgical evaluation and management of upper extremity spasticity in adults by Christopher S. Crowe, Paula A. Pino and Peter C.
Christopher S. Crowe (1887055), Peter C. Rhee and the Upper Extremity Spasticity Working Group (16998357), Paula A. Pino (16998354)   +2 more
core   +1 more source

Systematic Cardiac Phenotyping of Patients With Copy Number Variants in the 15q11.2 Breakpoint 1 to Breakpoint 2 Region: A Retrospective Cohort Study From Nine Pediatric Cardiac Centers

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Microdeletions impacting 15q11.2 breakpoint (BP) 1 to BP2, adjacent to the Prader–Willi critical region, have previously described neuropsychiatric associations, with potential low penetrance presentations of congenital heart disease (CHD) also identified.
Morgan B. Wright, Maria B. Padua, Lindsey R. Helvaty, Kim L. McBride, Gabrielle Geddes, Vidu Garg, Seema R. Lalani, Stephanie Burns Wechsler, Jennelle C. Hodge, Benjamin J. Landis, Stephanie M. Ware   +10 more
wiley   +1 more source

Current clinical practice of Irish physiotherapists and occupational therapists in the assessment and treatment of spasticity in adults [PDF]

Irish Journal of Occupational Therapy
Purpose – This paper aims to understand the clinical practice of physiotherapists and occupational therapists in the Republic of Ireland in the assessment and treatment of spasticity in adults, to inform and improve spasticity management practice.
Deirdre Manning, Mairead Campbell, Frances Horgan   +2 more
doaj   +1 more source

Genetic Variants of Na+,K+‐ATPase Associated With Neurological Disorders: A Systematic Review

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT Neurological disorders encompass a wide range of severe symptoms and manifestations, many of which are associated with genetic variants that affect ionic homeostasis. Na+,K+‐ATPase, a transmembrane enzyme responsible for maintaining electrochemical gradients in cells, plays a crucial role in neuronal excitability and brain function.
Giovana Kummer da Rosa, Leandro Rodrigo Ribeiro, Jéssica Lorena Bariviera, Mauro Schneider Oliveira   +3 more
wiley   +1 more source

Spasticity [PDF]

Canadian Medical Association Journal, 2014
Raphael, Rush, Dinesh, Kumbhare
openaire   +2 more sources

The EXPLAIN Study: Exploring Arthrogryposis Multiplex Congenita in Adults in Norway — A Description of Demographic, Medical, and Neurological Findings

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Arthrogryposis Multiplex Congenita (AMC) encompasses several hundred conditions with diverse genetic, pathophysiological, and clinical origins. The overarching EXPLAIN study explores underlying causes and implications of AMC and represents the largest clinical cohort of adults with AMC reported to date.
My Vuong Hermansen, Kristin Ørstavik, Unni Steen, Mathias Toft, Cathrine Brunborg, Lena Lande Wekre   +5 more
wiley   +1 more source

Assessment of seating forces imparted through daily activity by children with special needs [PDF]

, 2012
Extensor spasms regularly occur in spastic Cerebral Palsy (CP) children making their bodies unbalanced and causing wheelchair instability. Furthermore the child may be uncomfortable as a result of the high contact forces potentially causing pain and ...
Samaneein, Katika, Riches, Philip, Lees, Karl, Greene, Peter   +3 more
core   +3 more sources

Arthrogryposis Multiplex Congenita in Pediatric Age: Correlation Between MUScular MRI and Functional Evaluation (AMUSE), Toward a Biomechanical Model

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Arthrogryposis Multiplex Congenita (AMC) is a group of diseases with joint limitations at two or more distinct joint levels at birth. Joint limitations are not progressive, but the functional consequences have a lifelong impact on patients. The management of these conditions is therefore demanding, necessarily multidisciplinary, and is a long ...
Alicia‐Marine Milot, Mariya Raykova, Claire Huzar, Véronique Thellier, Nicolas Hergibo, Marjolaine Gauthier, Gipsy Billy‐Lopez, Chantal Durand, Frédérique Nugues, Véronique Bourg, Klaus Dieterich   +10 more
wiley   +1 more source

sj-pdf-1-jhs-10.1177_17531934231192843 - Supplemental material for Expert consensus on the surgical evaluation and management of upper extremity spasticity in adults

, 2023
Supplemental material, sj-pdf-1-jhs-10.1177_17531934231192843 for Expert consensus on the surgical evaluation and management of upper extremity spasticity in adults by Christopher S. Crowe, Paula A. Pino and Peter C.
Christopher S. Crowe (1887055), Peter C. Rhee and the Upper Extremity Spasticity Working Group (16998357), Paula A. Pino (16998354)   +2 more
core   +1 more source