Results 41 to 50 of about 799,164 (305)

Multiple follicular abnormalities in a 1‐year old cat consistent with basaloid follicular hamartomas [PDF]

, 2022
International audienceBackground: In humans, basaloid follicular hamartomas are benign follicular tumours, that can be solitary or multiple, in which case they show autosomal dominant inheritance.Hypothesis/Objectives: This study describes clinical and ...
Jérôme Abadie, Gaide, Nicolas, Abadie, Jérôme, Demorieux, Véronique, Semin, Marie, Marie O. Semin, Véronique Demorieux, Nicolas Gaide, Marie C. Cadiergues, Delverdier, Maxence, Cadiergues, Marie, Fabien Moog, Marinovic, Lucrecija, Lucrecija Marinovic, Moog, Fabien, Degorce-Rubiales, Frédérique, Maxence Delverdier, Zacharopoulou, Maria, Frédérique Degorce‐Rubiales, Maria Zacharopoulou   +19 more
core   +1 more source

Feasibility and Safety of Somato‐Cognitive Coordination Therapy for Cerebellar Ataxia Following Pediatric Brain Tumor Treatment

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Background Cerebellar ataxia after pediatric brain tumor treatment can cause persistent gait, balance, and speech impairment, yet no established rehabilitation strategy exists. Somato‐cognitive coordination therapy (SCCT) is a virtual reality–guided intervention designed to promote sensorimotor integration through visually constrained reaching
Masanobu Takeuchi, Takashi Matsuzawa, Jun Yamanishi, Masahiro Yoshitomi, Junji Ikeda, Shin‐Ichi Tsujimoto, Yasuteru Yamaguchi, Norio Shiba, Dhroov Pathare, Ayumi Kato, Masahiko Hara   +10 more
wiley   +1 more source

Abnormalities in normal-appearing white matter from which multiple sclerosis lesions arise [PDF]

, 2021
Normal-appearing white matter is far from normal in multiple sclerosis; little is known about the precise pathology or spatial pattern of this alteration and its relation to subsequent lesion formation.
Zhu, Bing, Geurts, Jeroen J. G., Fisher, Elizabeth, Elliott, Colm, Momayyezsiahkal, Parya, Liu, Dawei, Arnold, Douglas L., Belachew, Shibeshih, Cahir-Mcfarland, Ellen, Franchimont, Nathalie, Bradley, Daniel P., Gafson, Arie, Zhu, Li, Stys, Peter K., George, Ilena C., Ke, Jun   +15 more
core   +1 more source

KlippelFeil syndrome and associated congenital abnormalities: evaluation of 23 cases

Acta Orthopaedica et Traumatologica Turcica, 2020
Objectives: The purpose of this study was to review adult patients with Klippel-Feil syndrome.\nMethods: The study included 23 male patients (mean age 20.5 years, range 19 to 27 years) with Klippel-Feil syndrome.
Mahir ogullari, Huseyin Ozkan, Nadir Yildirim, Feridun Cilli, Etfal Gudemez   +4 more
doaj  

Sustained Therapeutic Efficacy of Intravenous Plasminogen Concentrate in Pediatric Patients With Type 1 Plasminogen Deficiency: An Analysis of Dosing Parameters and Clinical Outcomes

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Background Type 1 plasminogen deficiency (PLGD‐1) is an ultra‐rare autosomal recessive disorder caused by variants in the PLG gene and affects approximately 1.6 individuals per million. The condition is characterized by decreased plasminogen levels and impaired function, resulting in fibrin‐rich lesions on mucous membranes throughout the body.
Charles Nakar, Karen Thibaudeau, Mary Mathias, Heather McDaniel, Madlen Reschke, Klaus Tenbrock, Joseph M. Parker, Amy Shapiro   +7 more
wiley   +1 more source

Tear Abnormalities in Multiple Sclerosis [PDF]

, 1986
There is an extensive literature that implicates both cell-mediated and humoral mechanisms in the pathogenesis of multiple sclerosis(MS). Despite tremendous research efforts and the documentation of extensive immunologic abnormalities, its etiology and ...
Patrick A. Sibony, MD; P. K. Coyle, MD
core  

Multiple congenital ocular abnormalities (MCOA) in Rocky Mountain Horses and Kentucky Mountain Saddle Horses in Europe [PDF]

, 2010
The study describes the prevalence of multiple congenital ocular abnormalities (MCOA) in Rocky Mountain Horses and Kentucky Moutain Saddle Horses in Europe. Materials and methods: 35 RMH und KMSH were examined between 1999 and 2010. Their coat color were
Spiess, B M, Kaps, S
core   +1 more source

An aberrant bald eagle (Haliaeetus leucocephalus) with multiple anatomical abnormalities

Vertebrate Anatomy, Morphology, Palaeontology, 2019
Genetic abnormalities, especially polydactyly, are quite common among birds. Although there are numerous accounts of anatomically abnormal birds with polydactyly, few written anatomical descriptions have elucidated whether or not these physical ...
Jeremy Klingler, Christine Glasmann
doaj   +3 more sources

Health Literacy, Self‐Efficacy and Knowledge of Sickle Cell Disease Among Caregivers

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Background Sickle cell disease (SCD) is a hereditary blood disorder in which abnormal haemoglobin leads to severe anaemia, painful crises and organ failure. Caregivers’ health literacy (HL) – their ability to assess, understand and apply information, and interact with healthcare professionals – is crucial for managing children with SCD, yet ...
Melanie Bruinooge, Maite E. Houwing, Rowena L. Grohssteiner, Ferdows Atiq, Sonja A. M. C. Teuben, Mirjam P. Fransen, Marjon H. Cnossen   +6 more
wiley   +1 more source

Sexual dysfunction and sympathetic skin response recorded from the genital region in women with multiple sclerosis [PDF]

, 2007
Multiple Sclerosis is known to cause autonomic and sexual dysfunction. However, genitourinary and sexual problems in female multiple sclerosis patients are difficult to analyse. Therefore, it is an understudied field.
Kendir, Aysen Inceoglu, Tokucoglu, Figen, Basoglu, Mustafa, Arpaci, Esra, Gedizlioglu, Muhtesem, Secil, Yaprak, Yetimalar, Yesim, Ertekin, Cumhur   +7 more
core   +1 more source