Results 51 to 60 of about 1,232,690 (211)
Neurourology and Urodynamics, EarlyView.ABSTRACT Background Achieving continence in patients with neurogenic bladder is a difficult goal especially when stress urinary incontinence (SUI) due to intrinsic sphincter deficiency is involved. Two techniques are commonly used in that setting, but they have never been directly compared: the artificial urinary sphincter (AUS) and the fascial ...
Alicia Blondeau +7 more
wiley +1 more source
The Audiologic and Otolaryngologic Phenotype in WHIM Syndrome
Otolaryngology–Head and Neck Surgery, EarlyView.Abstract Objective WHIM syndrome (warts, hypogammaglobulinemia, infections, and myelokathexis syndrome) is an ultra‐rare primary immunodeficiency disease caused by autosomal dominant hyperfunctional mutations in the chemokine receptor CXCR4. Otolaryngologists are frequently consulted to evaluate WHIM patients because of recurrent acute ear and sinus ...
Christopher K. Zalewski +7 more
wiley +1 more source
, 2010 Evidence suggests that developmental coordination disorder (DCD) co-occurs with attention deficit hyperactivity disorder (ADHD) and joint hypermobility syndrome (JHS).
Sparks, J. +5 more
core +1 more source
Acta Obstetricia et Gynecologica Scandinavica, EarlyView.This review quantifies the association between collagenopathies and spontaneous preterm birth, assessing their role in antenatal risk assessment. Marfan syndrome is significantly associated with an increased risk of spontaneous preterm birth (OR 2.71, 95% CI 2.23–3.30; p < 0.001; I2 = 41%) while evidence for Ehlers–Danlos syndrome is heterogeneous ...
Kensie Treacy +3 more
wiley +1 more source
Incidence of Joint Hypermobility Syndrome in Anxienty Patients [PDF]
, 2019 Author: Bc. Marie Zasadilová Title: Incidence of Joint Hypermobility Syndrome in Anxienty Patients Objectives: The aim of this study is to find out what ist he incidence of Joint hypermobility syndrome in the research group of probands with anxiety ...
Zasadilová, Marie
core
Comparative diagnostic challenges in two horses with skin fragility disorders
Equine Veterinary Education, EarlyView.Summary Hereditary equine regional dermal asthenia (HERDA) is an autosomal recessive connective tissue disorder of horses caused by a missense mutation (c.115G>A) in the peptidyl‐prolyl cis–trans isomerase B (PPIB) gene, resulting in defective collagen organisation.
M. Biolchi +8 more
wiley +1 more source
Evaluation of lower limb disability in joint hypermobility syndrome
, 2011 The aim of this study is to evaluate degree and possible major determinants of lower limb disability in joint hypermobility syndrome. Forty patients with joint hypermobility syndrome were studied.
CASTORI, MARCO +5 more
core +1 more source
Journal of Rehabilitation, 2010 Objective: Numerous studies showed increasing incidence of acute or recurrent dislocations of the shoulder joint in people with General Hypermobility Syndrome (GHS). Given the critical role of scapular orientation in function of shoulder, the aim of this
Salman Nazary-Moghadam +3 more
doaj
Coexistence of Ankylosing Spondylosis with Benign Joint Hypermobility Syndrome. Are they Complementary to Each Other? [PDF]
Indian Journal of Physical Medicine & Rehabilitation, 2007 Objective: To present cases of co-existence of pathologically opposite conditions ankylosing spondylitis (AS) and benign joint hypermobility syndrome (BJHS).Design: Clinical findings of 25 cases of ankylosing spondylitis with overlapping clinical picture
Nallegowda M, Singh U, Khanna M, Kumar R
doaj
Headache: The Journal of Head and Face Pain, EarlyView.Abstract Background Occipital neuralgia (ON) is well characterized in adults but remains poorly understood in children. Pediatric ON may present with overlapping headache features and variable treatment responses, creating diagnostic and management challenges.
Miriam Meghnagi +8 more
wiley +1 more source