Results 181 to 190 of about 1,557,731 (346)

Adolescents' discourse on the consumption of psychoactive substances in schools. [PDF]

Rev Bras Enferm
Vasconcelos KNF, Lima HP, Aratani N, Giacon-Arruda BCC, Rozza SG, Silva SLVD, Brasil EGM, Nobre FMS.   +7 more
europepmc   +1 more source

Descriptive Epidemiology From the Myhre Syndrome Foundation Registry: The Value of Self‐Reported Data

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
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, Armelle Pindon, Maggie R. Brand, Kate Wears, Katherine H. Young, Alyssa Mendel, Michael J. Lyons   +6 more
wiley   +1 more source

Esclerosis Sistémica Juvenil con Afectación del Sistema Nervioso Central: Reporte de Caso

Revista Reumatología al Día
La esclerosis sistémica juvenil (ESJ) es una enfermedad rara del tejido conectivo, de origen desconocido, caracterizado por aumento del depósito de colágeno que produce fibroris y degeneración de la piel y de órganos internos.
Elizabeth Nicole Garzón Palacios, Richard Loor Chávez, Álvaro Nicolay Astudillo Mariño   +2 more
doaj  

Transition personnelle chez des adolescentes musulmanes vivant en France

, 2001
Hélène Chauchat, Khalid Boudarse
openalex   +2 more sources

Infantile‐Onset Ascending Hereditary Spastic Paraplegia due to a Homozygous ALS2 Exons 24–25 Deletion: Expanding the Genotypic Spectrum

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT We describe a novel homozygous intragenic deletion in the ALS2 gene in an 8‐year‐old boy with Infantile‐onset Ascending Hereditary Spastic Paraplegia (IAHSP) and oculomotor apraxia, thereby contributing to the expanding genetic landscape of ALS2‐related disorders.
Vito Luigi Colona, Maria Gnazzo, Silvia Genovese, Gessica Vasco, Lorena Travaglini, Maurizio Sabbadini, Marina Macchiaiolo, Francesco Nicita, Jacopo Sartorelli, Carmelo Piscopo, Enrico Castelli, Enrico Bertini, Andrea Bartuli, Antonio Novelli, Gessica Della Bella, Davide Vecchio   +15 more
wiley   +1 more source

Menstrual health: an analysis of experiences among school-aged adolescents. [PDF]

Rev Esc Enferm USP
Adomaitis JCO, Stofel NS, Silva MGF, Santos VC, Borges FA, Carlos DM, Farias BLS, Ogata MN, Monteiro JCDS.   +8 more
europepmc   +1 more source

Adjustment among Adolescents of Guwahati City in Relation to Gender and Religion

, 2019
Tahera Hoque Mozumdar, Indranee Phookan Borooah   +1 more
openalex   +2 more sources

Psychiatric Comorbidities and Treatment Modalities in Children With Osteogenesis Imperfecta: A Systematic Review of Mental Health

American Journal of Medical Genetics Part A, EarlyView.
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, Camille F. Villar, Beatriz Varman, Gianna M. Colombo, Danqi Li, Sarah J. Sadek, Marie‐Eve Robinson, Chaya N. Murali, Kara Ayers, Jocelyn Gomez, Brendan Lee, V. Reid Sutton, Eric A. Storch, Andrew D. Wiese   +13 more
wiley   +1 more source

Brugada Syndrome: New Implications for Heterozygous Carriers of the Pathogenic SCN5A c.689T>C(p.Ile230Thr) Variant

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Pathogenic variants in the SCN5A gene and its subunits have been identified in individuals with Brugada Syndrome. One such SCN5A variant, c.689T>C(p.Ile230Thr), was previously reported as disease‐causing only in homozygous individuals, with heterozygous carriers being unaffected.
Shayla Shojaat, Benjamin Hale, Taylor Warner   +2 more
wiley   +1 more source

EUPI-a: Escala de Uso Problemático de Internet en adolescentes. Desarrollo y validación psicométrica

, 2015
A. R. Boubeta, P. G. Salgado, M. I. Folgar, M. A. Gallego, Jesús Varela Mallou   +4 more
semanticscholar   +1 more source