Results 151 to 160 of about 114,297 (258)

Correlation of <i>UGT1A1</i> genotypes with newborn hyperbilirubinemia using newborn genetic screening. [PDF]

Front Pediatr
Ji Q, Zeng W, Li X, Chong S, Zhu J.
europepmc   +1 more source

A novel heterozygous mutation in ANK1 solves a mystery of a patient with hyperbilirubinemia and splenomegaly. [PDF]

Pak J Med Sci
Shi Y, Ou Y, Wu H.
europepmc   +1 more source

Case Report: Persistent indirect hyperbilirubinemia caused by Gilbert syndrome misdiagnosed as drug-induced liver injury during tuberculosis treatment. [PDF]

Front Med (Lausanne)
Liu P, Xu Y.
europepmc   +1 more source

Kernicterus Continues to Occur in the USA Despite Concerted Preventive Efforts. [PDF]

Case Rep Pediatr
Zeiler BB, Bahr TM, Ohls RK, Christensen RD.   +3 more
europepmc   +1 more source

Key role of Levitt's carbon monoxide breath test in revealing coexistent Gilbert syndrome and erythropoietic protoporphyria: A case report. [PDF]

World J Clin Cases
Kang LL, Zhang HD.
europepmc   +1 more source

Case Report: Therapeutic plasma exchange for severe unconjugated hyperbilirubinemia with bilirubin-induced neurologic dysfunction in an adolescent with Crigler-Najjar syndrome type II. [PDF]

Front Pediatr
Jaber M, Abuzahra A, Karajat AK, Abu Shama'a B, Hunyhen LK, Baradia L, Muhtasib L, Alzughayyar A, Hroob HIH, Dwaik M, Al-Takrori Y.   +10 more
europepmc   +1 more source

Case Report: Coexisting Hereditary Spherocytosis, Limited Cutaneous Systemic Sclerosis, and Antiphospholipid Syndrome: A Rare Autoimmune-Hemolytic Association. [PDF]

Int J Rheum Dis
Kumar DA, Rajamurugan PSA, Ramesh S, Mahadevan S, Kannan D.   +4 more
europepmc   +1 more source

Expert Consensus on the Diagnosis and Management of Inherited Hyperbilirubinemia (2025). [PDF]

J Clin Transl Hepatol
Zheng S, Xu X, Nan Y, Hou W, Bai J, Tang S, Liang C, Luo L, Wang J, Li X, Zhang M, Deng G, Liu H, Yang Y, Xie W, Ou X, Zhang X, Wei L, Jia J, Duan Z, Inherited Metabolic Liver Disease Collaboration Group, Chinese Society of Hepatology, Chinese Medical Association.   +22 more
europepmc   +1 more source

Case Report: Early recognition of neonatal alpha-1 antitrypsin deficiency: a case of subtle presentation and prompt diagnosis. [PDF]

Front Pediatr
James V, Darling S, Chin C, Bajwa P, Pillay A, Chu J, Gurevich Y, Kamath V.   +7 more
europepmc   +1 more source

Predisposing Factors for Congenital Hearing Loss: A Comprehensive Systematic Review. [PDF]

Turk Arch Otorhinolaryngol
Lalchandani T, Agarwal AC, Tiwari S.
europepmc   +1 more source