Results 161 to 170 of about 5,107,026 (330)
ABSTRACT Myhre syndrome is an ultrarare genetic disease characterized by short stature, distinct craniofacial features, cardiovascular and respiratory fibrosis and stenosis, neurodevelopmental delays, autism, intellectual disability, and hearing loss. The natural history of Myhre syndrome is still not fully understood due to a small patient population ...
Mary K. Young +6 more
wiley +1 more source
Differences in vaginal microbiome in African American women versus women of European ancestry.
Jennifer M. Fettweis +9 more
semanticscholar +1 more source
Dialogue and Involvement: A Blueprint for Human, Humane and Harmonious Relation Between African Americans and Africans [PDF]
Paul Ikechukwu Ogugua
openalex +1 more source
ABSTRACT To evaluate the prevalence of psychiatric signs and symptoms and describe psychotherapeutic and psychopharmacological interventions among children with osteogenesis imperfecta (OI). PRISMA guidelines were followed, and the study was registered in PROSPERO (CRD42024588284). Studies (n = 1419) were identified across five databases.
Julia M. Morales +13 more
wiley +1 more source
Meta-Analysis of the Gut Microbiome: An African American Representation. [PDF]
Kc A, Paudel R.
europepmc +1 more source
Incidence of Fluoroquinolone-Resistant and Extended Spectrum Beta-Lactamase Producing Escherichia coli in African American Males After Transrectal Ultrasound-Guided Prostate Biopsies [PDF]
Ali Kazerouni Timsar +4 more
openalex +1 more source
Genetic and Phenotypic Features of the Five Known Polyaminopathies: A Critical Narrative Review
ABSTRACT Polyaminopathies are a recently described family of rare genetic neurodevelopmental disorders. Polyaminopathies disrupt the biosynthesis of the primary polyamines: putrescine, spermidine, and spermine. Snyder–Robinson syndrome results from hemizygous loss‐of‐function variants in the spermine synthase (SMS) gene, resulting in decreased or ...
Elizabeth A. VanSickle +26 more
wiley +1 more source

