Results 21 to 30 of about 11,358 (182)

Movement Disorders in Developmental and Epileptic Encephalopathies

Movement Disorders Clinical Practice, EarlyView.
Abstract Background Monogenic developmental and epileptic encephalopathies (DEE) frequently feature co‐occurring movement disorders. Gene discovery has expanded epilepsy‐dyskinesia syndromes (EDS) from classic associations such as stereotypies in Rett syndrome to PRRT2‐related infantile seizures with paroxysmal dyskinesia and crouched gait in SCN1A ...
Shekeeb Mohammad, Darius Ebrahimi‐Fakhari, Hugo Morales‐Briceno   +2 more
wiley   +1 more source

La criptosporidiosis en niños hospitalizados. Hospital Provincial Pediátrico "Pepe Portilla" Cryptosporidiosis in hospitalized infants . "Pepe Portilla" Provincial Pediatric Hospital

Revista de Ciencias Médicas de Pinar del Río, 2012
Introducción: la Cryptosporidium ocasiona diarrea aguda, acuosa, no sanguinolenta y que puede acompañarse de anorexia , náusea s o vómitos y dolor abdominal.
Sandra Hernández García, Luis Montes de Oca, Odalys Cáceres Roque, Miguel Ángel Rodríguez Arencibia, Miguel Ángel Rodríguez Hernández   +4 more
doaj  

Effective prophylaxis against rotavirus diarrhea using a combination of Lactobacillus rhamnosus GG and antibodies

BMC Microbiology, 2007
Background Rotavirus is a worldwide cause of infectious infantile diarrhea that claims over 600,000 lives annually. Recently, two new vaccine candidates have been developed but their efficacy in developing countries, still remains to be proven.
Hammarström Lennart, Svensson Lennart, Brüssow Harald, Marcotte Harold, Pant Neha   +4 more
doaj   +1 more source

Precision Medicine in Neurodegeneration with Brain Iron Accumulation (NBIA) Disorders: An Update on Emerging Treatments

Movement Disorders Clinical Practice, EarlyView.
Abstract Background Neurodegeneration with Brain Iron Accumulation (NBIA) is a heterogeneous group of heritable, mostly recessive, progressive neurodegenerative diseases characterized by iron deposition in the basal ganglia and brainstem. There are no solid global epidemiological data on prevalence and incidence of NBIA subtypes, but registry data and ...
Susanne A. Schneider, Divyani Garg, Vassilena Iankova, Thomas Klopstock   +3 more
wiley   +1 more source

Chronic diarrhea and skin hyperpigmentation: A new association

The Saudi Journal of Gastroenterology, 2008
Background/Aims: The objective of this study was to describe patients with chronic diarrhea and abnormal skin hyperpigmentation with distinct distribution.
Al Qoaer Khaled, Al Mehaidib Ali, Shabib Sohail, Banemai Mohammed   +3 more
doaj  

Predominant enteropathogens in acute diarrhea and associated variables in children at the Lambayeque Regional Hospital, Peru [PDF]

Horizonte Médico, 2017
Objective: To determine the type and frequency of predominant enteropathogens in acute diarrhea and their associated characteristics in children treated at Hospital Regional Lambayeque (HRL) - Peru.
Heber Silva-Díaz, Olinda Bustamante-Canelo, Franklin-Rómulo Aguilar-Gamboa, Katya Mera-Villasis, Jhonatan Ipanaque-Chozo, Eberth Seclen-Bernabe, Martha Vergara-Espinoza   +6 more
doaj  

Diarréia por parasitas Parasites induced diarrheas

Revista Brasileira de Saúde Materno Infantil, 2002
A diarréia é uma causa importante de morbimortalidade nos países em desenvolvimento. Os agentes etiológicos mais comuns são os vírus e as bactérias. Este artigo tem o objetivo de analisar a ocorrência de diarréia como manifestação clínica de parasitose ...
Maria Eugênia Farias Almeida Motta, Gisélia Alves Pontes da Silva   +1 more
doaj   +1 more source

Review of nutrition management of pediatric intestinal pseudo‐obstruction

Nutrition in Clinical Practice, EarlyView.
Abstract Chronic intestinal pseudo‐obstruction (CIPO) is a rare, heterogeneous, and debilitating disorder characterized by profound intestinal dysmotility and severe nutrition challenges. Its presentation resembles that of mechanical bowel obstruction, but CIPO occurs in the absence of luminal obstruction.
Senthilkumar Sankararaman, Raisa Rani James, Bushra El‐Amaireh, Andrea Adler, Kadakkal Radhakrishnan, Sujithra Velayuthan   +5 more
wiley   +1 more source

Intestinal lymphangiectasia in a patient with infantile systemic hyalinosis syndrome: a rare cause of protein-losing enteropathy

Annals of Saudi Medicine, 2012
Infantile systemic hyalinosis (ISH) is a rare autosomal recessive disease. Typically, ISH patients present with progressive painful joint contractures, intractable diarrhea, hyperpigmented skin lesions, and perianal fleshy nodules.
Khalid Alreheili, Ali AlMehaidib, Khalid Alsaleem, Mohammad Banemi, Wajeeh Aldekhail, Sulaiman M. Al-Mayouf   +5 more
doaj   +1 more source

Iron Physiology and Its Impact on Atopic Diseases: An EAACI Taskforce Report

Allergy, EarlyView.
ABSTRACT Iron is essential for oxygen transport, energy metabolism, and immune regulation. Yet iron deficiency is the most common micronutrient disorder across all age groups, affecting nearly one quarter of the global population. Iron deficiency triggers nutritional immunity, a host defense mechanism that withholds and redistributes iron, contributing
Franziska Roth‐Walter, Ioana Agache, Beatriz Cabanillas, Roberto Berni Canani, Pasquale Comberiati, Holger Garn, Cristina Gomez‐Casado, Karin Hufnagl, Ekaterina Khaleva, Gregorio P. Milani, Daniel Munblit, Nikolaos Douladiris, Liam O'Mahony, Frank Redegeld, Carmen Riggioni, Peter K. Smith, Betty van Esch, Emilia Vassilopoulou, Carina Venter, Diego G. Peroni   +19 more
wiley   +1 more source