Results 181 to 190 of about 1,279,602 (365)

Family caregiver role in care recipient preparedness for hospital discharge: A parallel mediation model. [PDF]

PLoS One
Rayan-Gharra N, Tonkikh O, Gur-Yaish N.
europepmc   +1 more source

Hospitalization for Suicide Ideation or Attempt: 2008–2015

Pediatrics, 2018
Gregory Plemmons, M. Hall, Stephanie K. Doupnik, J. Gay, Charlotte M. Brown, Whitney L. Browning, R. Casey, Katherine L. Freundlich, David P. Johnson, Carrie Lind, Kris P. Rehm, Susan Thomas, Derek J. Williams   +12 more
semanticscholar   +1 more source

Case Report: Hypomyelinating Leukodystrophy Type 20 (HLD20) With Novel CNP Gene Variant

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT This case report describes a child with hypomyelinating leukodystrophy type 20 (HLD20), a rare neurodegenerative disorder characterized by impaired myelin formation. The patient presented with multiple neurodevelopmental abnormalities, including delayed motor milestones, seizures, and abnormal facial features.
Malak Alghamdi, Ghaida Alghamdi, Khalid Hundallah, Dima Jamjoom, Naif Almontashiri, Essa Alharbi, Muhammad Umair, Majid Alfadhel   +7 more
wiley   +1 more source

Heterogeneity of regional and national hospitalization burden of lupus nephritis and systemic lupus erythematous. [PDF]

Clin Kidney J
Avello A, Fernández-Prado R, Abasheva D, Mahillo I, González-Gay MÁ, Martín-Cleary C, Arce-Obieta JM, Pérez-Gómez MV, Fernández-Fernández B, Ortiz A.   +9 more
europepmc   +1 more source

Differences in Bacteriological and Antibiotic Sensitivity Patterns in UTI among Hospitalized Diabetic and Nondiabetic Patients

, 1970
Mohammed Kamrul Hasan, Khwaja Nazimuddin, AKM Shaheen Ahmed, Rene Suzan Claude Sarker, Muzammel Haque, AKM Musa   +5 more
openalex   +2 more sources

On Hospitalism [PDF]

BMJ
openaire   +2 more sources

Case Report: Unusual Neurological Features of Leigh Syndrome due to m.8993T>G Pathogenic Variant in the MT‐ATP6 Gene

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The MT‐ATP6 gene m.8993T>G pathogenic variant has been associated with Leigh syndrome, especially in patients exhibiting a high degree of heteroplasmy. Although patients may present with a wide phenotypic spectrum, characteristic findings include bilateral, symmetric hyperintensities in the basal ganglia and brainstem on brain MRI ...
Ramya Treitel, Julie McLaughlin, Marta Frigeni   +2 more
wiley   +1 more source

Identifying hospitalization episodes of care among people with and without HIV in British Columbia, Canada. [PDF]

BMC Med Res Methodol
Emerson SD, McLinden T, Sereda P, Trigg J, Yonkman AM, Salters KA, Au S, Kooij KW, Budu MO, Lima VD, Barrios R, Hogg RS.   +11 more
europepmc   +1 more source

Survivorship of Individuals With Double Heterozygosity for Achondroplasia and Type 2 Collagenopathy

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Historically, double heterozygosity, or a diagnosis of two separate, dominant genetic conditions, was often thought to be lethal in individuals with autosomal dominant skeletal dysplasias. In previously published studies of individuals with dual dysplasia diagnoses of achondroplasia and type 2 collagenopathy, infants died of respiratory ...
Valerie R. Schwartz, Andrea Schelhaas, Angela L. Duker, Ricki S. Carroll   +3 more
wiley   +1 more source

Factors associated with hospitalization from a geriatric short-stay unit (OBI-GER): a retrospective cohort study. [PDF]

Aging Clin Exp Res
Orlandini L, Maisano B, Ornago AM, Pinardi E, Finazzi A, Bonini A, Corsi M, Mosca G, Contro E, Staglianò A, Manna M, Piscitelli A, Andreassi A, Ferrara MC, Okoye C, Bellelli G.   +15 more
europepmc   +1 more source