Results 191 to 200 of about 1,397,270 (265)

Foundation Doctors' Understanding of Hospital Chaplaincy as Part of Holistic Care: A Cross-Sectional Survey at a District General Hospital in the United Kingdom. [PDF]

Cureus
Chiu HYJ, Donnelly G.
europepmc   +1 more source

Spinal Involvement in Charge Syndrome: Implications for Management

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT CHARGE syndrome (OMIM #214800) is an autosomal dominant disorder caused by mutations in the CHD7 gene in most cases. Although originally defined by the CHARGE acronym (coloboma, heart defects, choanal atresia, growth restriction, genital hypoplasia, and ear anomalies), the recognized phenotype has expanded considerably to include highly ...
Adriana Gomes, Álvaro Martín‐Rodríguez, Miguel del Campo Casanelles, Marilyn C. Jones, Daniela Carvalho, Lynne M. Bird   +5 more
wiley   +1 more source

Correction to 'Multidisciplinary Perioperative Care of a One-Month-Old Infant With Severe Traumatic Brain Injury and Brain Herniation: A Case Report'. [PDF]

Nurs Crit Care
europepmc   +1 more source

From Crisis to Care: A Multidisciplinary Care Framework for Repatriated Civilian Hostages: Development, Implementation, and Early Outcomes. [PDF]

Healthcare (Basel)
Nutman A, Yosha Orpaz L, Oren S, Maor Y, Goldstein AL, Twito O, Menachemi D, Hovel D, Zohar I, Dayan K, Barda G, Levy A, Shpitzer Z, Levinberg L, Noah M, Zvi O, Engel A.   +16 more
europepmc   +1 more source

ADNP‐Related Helsmoortel–Van der Aa Syndrome: A Review of the Literature and Clinical Recommendations for Assessment and Monitoring

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT ADNP‐related Helsmoortel–Van der Aa syndrome (ADNP‐related HVDAS) is a single gene form of autism spectrum disorder (ASD) caused by pathogenic sequence variants in the activity‐dependent neuroprotective protein (ADNP) gene. In addition to ASD, ADNP‐related HVDAS is associated with a wide range of cognitive, behavioral, and physical health ...
Jarrett Fastman, Ana Kolevzon, Paige Siper, Tess Levy, Jeffrey M. Saland, Yitzchak Frank, Robert Rapaport, Kayla Kupietzky, William E. Bennett Jr, Bruce Gelb, Sandra Bedrosian Sermone, Alexander Kolevzon   +11 more
wiley   +1 more source

Five-year implementation and longitudinal performance of a multidisciplinary acute myocardial infarction program in a middle-income country. [PDF]

Int J Cardiol Cardiovasc Risk Prev
Pérez BM, Hurtado-Ortiz A, Gualteros Cely PA, Serrano JL, Angarita AB, Manrique-Hernández EF, Licht-Ardila M, Saiibi JF.   +7 more
europepmc   +1 more source

Severe Headbanging Responsive to Levodopa in a Child With FOXP1 Syndrome

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT We report a 9‐year‐old female with FOXP1 syndrome due to a de novo in‐frame deletion in the FOXP1 gene. The child has a severe neurodevelopmental disorder including global developmental delay and autism spectrum disorder. At age 2, she developed severe headbanging, which was progressive and did not respond to multidisciplinary, behavioral ...
Pamela Veale, Christopher Tiessen, Vithya Gnanakumar   +2 more
wiley   +1 more source

Disproportionate bulbar dysfunction following small corona radiata infarction in vascular parkinsonism: A case report. [PDF]

Medicine (Baltimore)
Wang HW.
europepmc   +1 more source