Results 281 to 290 of about 164,622 (370)

ADVERSE NEURODEVELOPMENTAL OUTCOME OF MODERATE NEONATAL HYPOGLYCEMIA [PDF]

, 1988
COLE, TJ, LUCAS, A, MORLEY, R
core  

Feasibility and clinical value of pyloric functional luminal imaging probe in an infant

JPGN Reports, EarlyView.
Abstract Pyloric dysfunction is becoming increasingly recognized as a cause of gastroparesis, but its diagnostic and therapeutic role in infants has not been well studied. Identification and treatment of pyloric dysfunction with functional luminal imaging probe (FLIP) technology or use of pyloric inhibition are not routinely used in infants due to lack
Ariel Porto, Roman S. Pantazopoulos, Peter T. Osgood, John E. Fortunato   +3 more
wiley   +1 more source

Accuracy and clinical effectiveness of fetal growth monitoring strategies for the prediction of small for gestational age at birth: a systematic review and meta-analysis.

Health Technol Assess
Danopoulos E, Armstrong N, McDermott K, Chen J, Tian X, Noake C, Westwood M.   +6 more
europepmc   +1 more source

Knowledge Gaps Regarding Overweight and Obesity in Pregnancy: A Cross-Sectional Study Among Polish Women. [PDF]

Nutrients
Froń A, Orczyk-Pawiłowicz M.
europepmc   +1 more source

Why is screening for neonatal hypoglycemia important in Small for Gestational Age (SGA) infants?

Tripdatabase
openalex   +1 more source

A retrospective cohort study evaluating the growth and clinical outcomes of preterm and term infants with cystic fibrosis during the first 11 years of life

JPGN Reports, EarlyView.
Abstract Objectives Infants with cystic fibrosis (iwCF) have lower birth weights than others. That influences nutritional and pulmonary outcomes. It was reported that 86.0% of iwCF were born full‐term and 14.0% preterm. Data on the role of gestational age in growth and clinical outcomes of people with cystic fibrosis (pwCF) is limited.
Hebah Reda, Sanjidah Ahmed, Julie Sturza, Samya Z. Nasr   +3 more
wiley   +1 more source

Maternal inflammatory biomarkers and neonatal characteristics as predictors of bronchopulmonary dysplasia in preterm infants: a retrospective cohort study. [PDF]

Front Med (Lausanne)
Liu Y, Fang C, Zhao S.
europepmc   +1 more source

Diagnostic dilemma of cystic biliary atresia: A series of two cases and brief review of the diagnostic modalities

JPGN Reports, EarlyView.
Abstract Cystic biliary atresia (CBA) is a rare variant of biliary atresia that closely resembles choledochal cyst (CC), complicating diagnosis and potentially delaying critical surgical intervention. We report two cases of CBA that were difficult to diagnose.
Hamza Hassan Khan, Leslie Hirsig Spence, Nagraj Kasi   +2 more
wiley   +1 more source

Impact of Prematurity and Maternal Bonding on Sensory Processing at 12 Months. [PDF]

Children (Basel)
Yildiz A, Yildiz R, Basaran Z, Atalan Efkere P, Zorlular R, Celik HI, Elbasan B.   +6 more
europepmc   +1 more source

PERCC1‐associated enteropathy: Diagnostic challenges and enteral autonomy achieved with teduglutide

JPGN Reports, EarlyView.
Abstract Congenital diarrheas and enteropathies (CODE) are rare inherited disorders characterized by early‐onset intractable diarrhea. Though progress has been made in elucidating the genetic basis of CODE, much remains to be discovered. Another challenge is the lack of curative therapies—treatment is primarily supportive including enteral and ...
Angela Tran, Vivien Nguyen, Phuong Huynh
wiley   +1 more source