Results 51 to 60 of about 168,012 (204)

Hand Foot and Mouth Disease in an infant [PDF]

open access: yes, 2020
Hand foot and mouth disease is a self limiting enteroviral lesion characterized by papulovesicular eruptions over hands and feet with circinate oral ulcers in the palate.
Chandrasekaran Venkatesh   +5 more
core  

Sentinel surveillance for enterovirus 71, Taiwan, 1998. [PDF]

open access: yes, 1999
Outbreaks of enterovirus 71 have been reported around the world since 1969. The most recent outbreak occurred in Taiwan during April-July 1998. This hand, foot, and mouth disease epidemic was detected by a sentinel surveillance system in April at the ...
Alexander   +13 more
core   +2 more sources

Seguir adelante: A qualitative exploration of Latino farmworkers' work and nonwork resources

open access: yesAmerican Journal of Community Psychology, EarlyView.
Abstract Latino immigrant workers have been an exploited community within many dangerous workforces, but especially within the agricultural industry. They are a crucial population for the labor and economy of the U.S., yet Latino farmworkers report feeling expendable, discriminated against, and exposed to hazardous working conditions.
Faviola Robles Saenz   +3 more
wiley   +1 more source

Hand, foot and mouth disease in Guangdong, China, in 2013: new trends in the continuing epidemic [PDF]

open access: yes, 2014
Millions of incidents of hand, foot and mouth disease occur annually in China, with EVA71 and CVA16 as two major causative pathogens. A provincial surveillance system has been implemented in Guangdong for almost 5 years to analyze the aetiological ...
Guo, X.   +10 more
core   +1 more source

A Case of Prader‐Willi Syndrome With a Deletion Including MAGEL2, NDN, and MKRN3, but Excluding SNRPN and SNORD116

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Prader‐Willi syndrome (PWS) is a neurodevelopmental disorder typically caused by large deletions or imprinting defects on chromosome 15q11.2, encompassing multiple genes. While the contribution of individual genes to the PWS phenotype remains unclear, previous studies suggested that isolated deletions of MAGEL2, NDN, and MKRN3, excluding the ...
Jannis Buecking   +6 more
wiley   +1 more source

Acute Encephalitis Caused by Intrafamilial Transmission of Enterovirus 71 in Adult [PDF]

open access: yes, 2008
Enterovirus 71 (EV71) is a common cause of hand, foot, and mouth disease and sometimes causes severe neurologic complications, mainly in children. We report a case of adult-onset encephalitis caused by intrafamilial transmission of a subgenogroup C4 ...
Chan   +19 more
core   +2 more sources

Phenotypic Characterization of Seven Pediatric Patients Diagnosed With KAT6B‐Related Disorders: Case Series and Review of the Literature

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Genitopatellar syndrome (GPS) and Say‐Barber‐Biesecker‐Young‐Simpson Syndrome (SBBYSS) are clinically distinct neurodevelopmental disorders caused by monoallelic pathogenic variants in KAT6B. In some cases, GPS and SBBYSS features can overlap, determining an intermediate phenotype.
Vittorio Maglione   +12 more
wiley   +1 more source

Epidemic Hand, Foot and Mouth Disease Caused by Human Enterovirus 71, Singapore [PDF]

open access: yes, 2003
Singapore experienced a large epidemic of hand, foot and mouth disease (HFMD) in 2000. After reviewing HFMD notifications from doctors and child-care centers, we found that the incidence of HFMD rose in September and declined at the end of October ...
Ai Ee Ling   +29 more
core   +2 more sources

Addressing the Diagnostic Odyssey for Adults With Neurodevelopmental Disabilities: Case Study of an Individual With Mandibulofacial Dysostosis With Microcephaly

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Whole exome sequencing (WES) has been widely used in the pediatric setting to increase diagnostic yield, provide treatment options, and to estimate reoccurrence risks. However, there is limited knowledge regarding the utility of this technology in adults with neurodevelopmental disabilities.
Ruhi Shah   +6 more
wiley   +1 more source

Paroxysmal Supraventricular Tachycardia in an Infant with Hand, Foot, and Mouth Disease [PDF]

open access: yes, 2011
An 11-month-old male infant was admitted to our hospital with fever, fussiness, poor feeding, vomiting, and tachypnea for two days prior. Physical examination revealed sporadic papules and vesicles occurring on his hands, feet, face, and perianal mucosa.
Chan   +21 more
core   +3 more sources

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