Zobrazeno 1 - 10
of 191
pro vyhledávání: '"Rajeev Mehta"'
Publikováno v:
Case Reports in Genetics, Vol 2024 (2024)
3-hydroxy isobutyl-CoA hydrolase (HIBCH) deficiency is a recently described, rare inborn error of valine metabolism associated with a Leigh syndrome-like phenotype, neurodegenerative symptoms, and caused by recessive mutations in the HIBCH gene. We r
Externí odkaz:
https://doaj.org/article/42fe97fa785b4959afd66cb86903600e
Publikováno v:
Pediatrics and Neonatology, Vol 64, Iss 2, Pp 160-167 (2023)
Background: The role of prematurity and pulmonary inflammation in the pathogenesis of bronchopulmonary dysplasia (BPD) is very well-defined. However, there is limited knowledge about whether the level of prematurity and surfactant therapy alter the p
Externí odkaz:
https://doaj.org/article/6a5fe65aa3f540b48b909a375646d0e0
Autor:
Rajeev Mehta, Anna Petrova
Publikováno v:
Pediatrics and Neonatology, Vol 62, Iss 4, Pp 406-411 (2021)
Background: This research evaluated the association between the mother-infant blood type or rhesus (ABO or Rh) incompatibility, the pattern of neonatal jaundice, and serum bilirubin (TSB) values obtained prior to discharge from hospital of healthy bo
Externí odkaz:
https://doaj.org/article/5e7e31ded9164e8f8869c01212196599
Autor:
Surasak Puvabanditsin, Michelle Gorbonosov, Kristin Blackledge, Jeffrey Manzano, Matthew Federici, Rajeev Mehta
Publikováno v:
Clinical Case Reports, Vol 10, Iss 7, Pp n/a-n/a (2022)
Abstract We report a preterm male neonate presenting with a short trunk, short neck, low hairline, deformed ears, preauricular skin tag, penoscrotal transposition (PT), palmar crease, short and broad fingers and toes (brachydactyly), hypoplastic and
Externí odkaz:
https://doaj.org/article/0e7bc77b5dd34698941bdda0e2ec337d
Autor:
Surasak Puvabanditsin, Miry Shim, Jeffrey Suell, Jeffrey Manzano, Kristin Blackledge, Avram Bursky-Tammam, Rajeev Mehta
Publikováno v:
Case Reports in Urology, Vol 2022 (2022)
We report a term male neonate presenting with a “prune belly,” bilateral hydronephrosis, hydroureter, posterior urethral obstruction, and bilateral undescended testes. Analysis with the whole genome SNP microarray revealed an interstitial deletio
Externí odkaz:
https://doaj.org/article/7622fb52d5fd4b8e9589b551e58ecfbd
Autor:
Surasak Puvabanditsin, Vidya Puthenpura, Seyni Gueye-Ndiaye, Michele Takyi, Adaora Madubuko, Lauren Walzer, Rajeev Mehta
Publikováno v:
Annals of Pediatric Cardiology, Vol 11, Iss 2, Pp 194-196 (2018)
We report a term female infant with congenital heart block and total anomalous of pulmonary venous return. The results of single nucleotide polymorphism oligonucleotide microarray analysis showed an interstitial duplication of approximately 818 Kb, w
Externí odkaz:
https://doaj.org/article/c9012be6e86946fa82a132052f8a00ac
Publikováno v:
PLoS ONE, Vol 14, Iss 4, p e0214683 (2019)
Despite the positive survival trend in infants born prematurely, the risk for development of intracranial lesions has remained unchanged. However, there are limitations to our understanding of the pattern of the magnetic resonance imaging (MRI) -dete
Externí odkaz:
https://doaj.org/article/1f72a5c190d84996956a2a45acfda6c6
Autor:
Surasak Puvabanditsin, Marianne Jacob, Maaz Jalil, Samhita Bhattarai, Qaiser Patel, Mehrin Sadiq, Rajeev Mehta
Publikováno v:
Case Reports in Infectious Diseases, Vol 2019 (2019)
We report a case of a 12-day-old term neonate with extended-spectrum beta-lactamase (ESBL) producing Escherichia coli (E. coli) meningitis and cerebral abscess. The patient received a 7-day course of antibiotics just few days prior to the infection.
Externí odkaz:
https://doaj.org/article/c3c5902ab12841eea6ea4f88e360f383
Publikováno v:
Nutrients, Vol 12, Iss 6, p 1571 (2020)
Breastfeeding has been recommended for preterm infants as the optimal diet from nutritional, gastrointestinal, immunological, and developmental perspectives. However, the relevance of differing intakes of fortified mother’s own milk (MOM) on the gr
Externí odkaz:
https://doaj.org/article/8878cf262f7d41aeacfa40272552b12a
Publikováno v:
Case Reports in Pathology, Vol 2018 (2018)
We report a term male neonate with congenital myeloproliferative disorder, thrombocytopenia, a horseshoe kidney, feeding difficulty secondary to dysphagia/foregut dysmotility, and respiratory failure. Prenatal molecular genetic analysis revealed a fe
Externí odkaz:
https://doaj.org/article/f14b915dd464461c9f21d32d09622426