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Subject : hyperbilirubinemia, neonatal
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Academic Journal

Genetic Factors and Delayed TSB Monitoring and Treatment as Risk Factors Associated with Severe Hyperbilirubinemia in Term Neonates Admitted for Phototherapy.

  • Authors : Boo NY; Department of Population Medicine, Faculty of Medicine and Health Sciences, Universiti Tunku Abdul Rahman, Bandar Sungai Long, Selangor, Malaysia.; Sin S

Subjects: Bilirubin/Bilirubin/Bilirubin/*blood ; Glucosephosphate Dehydrogenase/Glucosephosphate Dehydrogenase/Glucosephosphate Dehydrogenase/*genetics ; Glucuronosyltransferase/Glucuronosyltransferase/Glucuronosyltransferase/*genetics

  • Source: Journal of tropical pediatrics [J Trop Pediatr] 2020 Dec 01; Vol. 66 (6), pp. 569-582.Publisher: Oxford University Press Country of Publication: England NLM ID: 8010948 Publication Model: Print Cited Medium: Internet ISSN:

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Academic Journal

SLCO1B1 c.388A > G variant incidence and the severity of hyperbilirubinemia in Indonesian neonates.

  • Authors : Amandito R; Neonatal Intensive Care Unit, Pondok Indah General Hospital, Jl Metro Duta Kav. UE, Pondok Indah, Jakarta, Indonesia. .; Division of Perinatology, Department of Child Health, Cipto Mangunkusumo General Hospital, Faculty of Medicine Universitas Indonesia, Jl Pangeran Diponegoro No. 71, Central Jakarta, Jakarta, Indonesia. .

Subjects: Polymorphism, Restriction Fragment Length*; Hyperbilirubinemia, Neonatal/Hyperbilirubinemia, Neonatal/Hyperbilirubinemia, Neonatal/*genetics ; Liver-Specific Organic Anion Transporter 1/Liver-Specific Organic Anion Transporter 1/Liver-Specific Organic Anion Transporter 1/*genetics

  • Source: BMC pediatrics [BMC Pediatr] 2019 Jun 28; Vol. 19 (1), pp. 212. Date of Electronic Publication: 2019 Jun 28.Publisher: BioMed Central Country of Publication: England NLM ID: 100967804 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2431

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Academic Journal

Combined effects of the UGT1A1 and OATP2 gene polymorphisms as major risk factor for unconjugated hyperbilirubinemia in Indian neonates.

  • Authors : D'Silva S; National Institute of Immunohaematology (ICMR), 13th floor, NMS Building, KEM Hospital Campus, Parel, Mumbai 400 012, India.; Colah RB

Subjects: Genetic Predisposition to Disease* ; Polymorphism, Single Nucleotide*; Glucuronosyltransferase/Glucuronosyltransferase/Glucuronosyltransferase/*genetics

  • Source: Gene [Gene] 2014 Aug 15; Vol. 547 (1), pp. 18-22. Date of Electronic Publication: 2014 May 24.Publisher: Elsevier/North-Holland Country of Publication: Netherlands NLM ID: 7706761 Publication Model: Print-Electronic Cited Medium: Internet

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Academic Journal

Neonatal hyperbilirubinemia and organic anion transporting polypeptide-2 gene mutations.

Subjects: Polymorphism, Single Nucleotide*; Hyperbilirubinemia, Neonatal/Hyperbilirubinemia, Neonatal/Hyperbilirubinemia, Neonatal/*genetics ; Liver-Specific Organic Anion Transporter 1/Liver-Specific Organic Anion Transporter 1/Liver-Specific Organic Anion Transporter 1/*genetics

  • Source: American journal of perinatology [Am J Perinatol] 2011 Sep; Vol. 28 (8), pp. 619-26. Date of Electronic Publication: 2011 Apr 15.Publisher: Thieme-Stratton Country of Publication: United States NLM ID: 8405212 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Variants of organic anion transporter polypeptide 2 gene are not risk factors associated with severe neonatal hyperbilirubinemia.

  • Authors : Wong FL; Unit of Haematology, Department of Diagnostic Laboratory Services, Universiti Kebangsaan Malaysia Medical Center, Kuala Lumpur, Malaysia.; Boo NY

Subjects: Genetic Predisposition to Disease* ; Polymorphism, Genetic*; Hyperbilirubinemia, Neonatal/Hyperbilirubinemia, Neonatal/Hyperbilirubinemia, Neonatal/*genetics

  • Source: The Malaysian journal of pathology [Malays J Pathol] 2009 Dec; Vol. 31 (2), pp. 99-104.Publisher: Academy of Medicine of Malyasia, College of Pathologists Country of Publication: Malaysia NLM ID: 8101177 Publication Model: Print Cited Medium:

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Academic Journal

Associations between UGT1A1, SLCO1B1, SLCO1B3, BLVRA and HMOX1 polymorphisms and susceptibility to neonatal severe hyperbilirubinemia in Chinese Han population.

  • Authors : Fan J; Department of Neonatology , Children's Hospital of Chongqing Medical University, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Child Rare Diseases in Infection and Immunity, Chongqing, China.; He HY

Subjects: Polymorphism, Single Nucleotide* ; Hyperbilirubinemia, Neonatal*/Hyperbilirubinemia, Neonatal*/Hyperbilirubinemia, Neonatal*/genetics; Infant, Newborn

  • Source: BMC pediatrics [BMC Pediatr] 2024 Jan 26; Vol. 24 (1), pp. 82. Date of Electronic Publication: 2024 Jan 26.Publisher: BioMed Central Country of Publication: England NLM ID: 100967804 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2431

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Academic Journal

Red Blood Cell Membrane-Related Gene Variants and Clinical Risk Factors in Chinese Neonates with Hyperbilirubinemia.

  • Authors : Lin F; Precision Medical Lab Center, Chaozhou Central Hospital Affiliated to Southern Medical University, Chaozhou, China.; Xu JX

Subjects: Hyperbilirubinemia, Neonatal*/Hyperbilirubinemia, Neonatal*/Hyperbilirubinemia, Neonatal*/genetics; Humans ; Infant, Newborn

  • Source: Neonatology [Neonatology] 2023; Vol. 120 (3), pp. 371-380. Date of Electronic Publication: 2023 Apr 11.Publisher: Karger Country of Publication: Switzerland NLM ID: 101286577 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Associations between UGT1A1 and SLCO1B1 polymorphisms and susceptibility to neonatal hyperbilirubinemia in Thai population.

  • Authors : Atasilp C; Chulabhorn International College of Medicine, Thammasat University, Pathum Thani, Thailand.; Kanjanapipak J

Subjects: Hyperbilirubinemia, Neonatal*/Hyperbilirubinemia, Neonatal*/Hyperbilirubinemia, Neonatal*/genetics ; Jaundice, Neonatal*/Jaundice, Neonatal*/Jaundice, Neonatal*/complications ; Jaundice, Neonatal*/Jaundice, Neonatal*/Jaundice, Neonatal*/genetics

  • Source: BMC pediatrics [BMC Pediatr] 2022 May 02; Vol. 22 (1), pp. 243. Date of Electronic Publication: 2022 May 02.Publisher: BioMed Central Country of Publication: England NLM ID: 100967804 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2431

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Academic Journal

[Research advances in neonatal hyperbilirubinemia and gene polymorphisms].

  • Authors : He CH; Department of Pediatrics, West China Second University Hospital/Key Laboratory of Birth Defects and Related Diseases of Women and Children (Sichuan University), Ministry of Education, Chengdu 610041, China. .; Qu Y

Subjects: Hyperbilirubinemia, Neonatal*/Hyperbilirubinemia, Neonatal*/Hyperbilirubinemia, Neonatal*/genetics ; Polymorphism, Genetic*; Bilirubin

  • Source: Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics [Zhongguo Dang Dai Er Ke Za Zhi] 2020 Mar; Vol. 22 (3), pp. 280-284.Publisher: Zhongguo dang dai er ke za zhi she Country of Publication: China NLM ID: 100909956 Publication Model: Print Cited Medium: Print ISSN:

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Academic Journal

Effect of genetic variants of bilirubin metabolism on the degree of hyperbilirubinemia in African-American newborns.

  • Authors : Schutzman DL; Department of Pediatrics and Adolescent Medicine, Einstein Medical Center, Philadelphia, PA, USA.; Baudhuin LM

Subjects: Black or African American/Black or African American/Black or African American/*genetics ; Bilirubin/Bilirubin/Bilirubin/*blood ; Bilirubin/Bilirubin/Bilirubin/*metabolism

  • Source: Journal of perinatology : official journal of the California Perinatal Association [J Perinatol] 2017 Apr; Vol. 37 (4), pp. 432-435. Date of Electronic Publication: 2016 Dec 15.Publisher: Nature Publishing Group Country of Publication: United States NLM ID: 8501884 Publication Model: Print-Electronic Cited Medium: Internet

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  • 1-10 of  20 results for ""Liver-Specific Organic Anion Transporter 1""