Results 281 to 290 of about 1,765,666 (345)

Genetic disorders and associated morbidity, mortality, and congenital anomalies in preterm infants born at less than 34 weeks of gestation. [PDF]

BMC Pediatr
Everett SS, Bomback M, Banerjee A, Sahni R, Wapner RJ, Tolia VN, Clark RH, Lyford A, Hays T.   +8 more
europepmc   +1 more source

Follow-up of neonatal chronic respiratory disease: an update based on the current evidence. [PDF]

Eur J Pediatr
Jenkinson A, Dassios T.
europepmc   +1 more source

Update on the infant supplementation with vitamin D3, vitamin K1 and DHA

Tena Niseteo
openalex   +1 more source

INFANT MALNUTRITION.

The Central African journal of medicine, 1964
openaire   +2 more sources

Nance‐Horan Syndrome: Further Delineation of the Affected Male and the Female Carrier Phenotypes

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Nance‐Horan syndrome (NHS; OMIM 302350) is a rare, X‐linked syndrome characterized by bilateral congenital cataracts leading to profound vision loss, specific dental anomalies including characteristic screwdriver blade‐shaped incisors, facial anomalies, and intellectual disability.
Maria K. Haanpää, Chad R. Haldeman‐Englert, Marja Hietala, Melisa S. Tanverdi, Patrick P. Koty, Diana Brightman, Eniolami Dosunmu, Shailja Tibrewal, Savleen Kaur, Anupriya Kaur, Raj Kumar Verma, Alejandra G. de Alba Campomanes, Virginia Utz, Anne M. Slavotinek, Cynthia Curry   +14 more
wiley   +1 more source

Early Detection and Hearing Intervention in Infants With Bilateral Moderate Hearing Loss: Based on a Nationwide Infantile Hearing Aid Support Program in Korea. [PDF]

J Korean Med Sci
Kim YS, Choo OS, Park SK, Park E, Choi J, Im GJ, Chang J.   +6 more
europepmc   +1 more source

Non‐RASopathy Genetic Syndromes Identified as the Molecular Cause of Disease in Patients Previously Diagnosed With Noonan Syndrome

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Noonan Syndrome (NS) is a clinically and genetically heterogeneous condition characterized by typical facial dysmorphisms, short stature, congenital heart defects, and developmental delays. While variants in genes such as PTPN11, SOS1, and RAF1 account for most genetically confirmed cases, diagnosis is challenging due to phenotypic overlap ...
Gabriela Jeesoo Kim, Alexsandra Christianne Malaquias, Debora Romeo Bertola, Raissa Carneiro Rezende, Laurana De Polli Cellin, Lucas Vieira Lacerda Pires, Ana Maria Santillan‐Vasconez, Antônio Marcondes Lerario, Renata da Cunha Scalco, Alexander Augusto de Lima Jorge   +9 more
wiley   +1 more source

Identifying Predictors for the Acquisition of Tolerance to Cow's Milk Protein in Infants with Food Protein-Induced Allergic Proctocolitis (FPIAP): Multifactorial Analysis of Two Italian Cohorts. [PDF]

Nutrients
Scavella A, Ferrigno C, Baù M, Colombo A, Tavernelli CI, Zobele M, Borgetto R, Maggi A, Baronti A, Francone A, Zuccotti GV, Agosti M, D'Auria E, Salvatore S.   +13 more
europepmc   +1 more source

Patent Ductus Arteriosus in Preterm Neonates: A 2025 Synthesis of Evidence-Based Paradigms and Emerging Clinical Strategies. [PDF]

Pediatr Discov
Bhatt AH, Nimbalkar SM, Patel DV, Pujara RK.   +3 more
europepmc   +1 more source

Trial protocol: DOLFIN trial: Developmental Outcomes of Long-term Feed Supplementation in Neonates-A UK multicentre, blinded, stratified, randomised controlled trial. [PDF]

Trials
Andrew MJ, Embleton N, Hardy P, Johnson S, Juszczak E, Ledbury H, Pearson C, Rivero-Arias O, Francisco AA, Berrington J, Bradley P, Bradley PJ, Cole C, Court K, Hurd M, King A, Linsell L, Murray D, O'Connor HM, Roehr CC, Stalker V, Stanbury K, Wahengbam UD, Welsh R, Wiles J, Parr JR.   +25 more
europepmc   +1 more source