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Demographics of tonsillar hypertrophy among sickle cell disease patients in calabar

Nigerian journal of clinical practice, 2023-07, Vol.26 (7), p.1023-1028

2023

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Bacterial Profile, Susceptibility Patterns, and Factors Associated with Culture-Positive Sputum Among HIV Patients Presenting with a Cough in Northern Uganda

HIV/AIDS (Auckland), 2024-09, Vol.16, p.355-366

2024

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Increased Incidence of Late-Onset Circulatory Collapse after Changing Clinical Practice: A Retrospective Investigation of Causative Factors

American journal of perinatology, 2015-10, Vol.32 (12), p.1169-1176

2015

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Molecular analysis of congenital central hypoventilation syndrome

Human genetics, 2003-12, Vol.114 (1), p.22-26

2003

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Cytogenetic studies of Hynobiidae (Urodela)

Cytogenetic and Genome Research, 2002-01, Vol.99 (1-4), p.194-199

2002

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Neonatal hyperbilirubinemia and mutation of the bilirubin uridine diphosphate‐glucuronosyltransferase gene: a common missense mutation among Japanese, Koreans and Chinese

Biochemistry and molecular biology international, 1998-09, Vol.46 (1), p.21-26

1998

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Cytogenetic studies of Hynobiidae (Urodela)XVIII. A ZZ/ZW sex-determining mechanism in a hynobiid salamander species, Hynobius tokyoensis Tago

Cytogenetic and genome research, 2002, Vol.99 (1-4), p.194-199

2002

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Intermittent jaundice in patients with acute leukaemia: A common mutation of the bilirubin uridine‐diphosphate glucuronosyltransferase gene among Asians

Journal of inherited metabolic disease, 1999-08, Vol.22 (6), p.747-753

1999

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Neonatal hyperbilirubinemia in Japanese neonates: Analysis of the heme oxygenase-1 gene and fetal hemoglobin composition in cord blood

Pediatric research, 2003-08, Vol.54 (2), p.165-171

2003

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Neonatal hyperbilirubinemia and the bilirubin uridine diphosphate-glucuronosyltransferase gene: The common −3263T > G mutation of phenobarbital response enhancer module is not associated with the neonatal hyperbilirubinemia in Japanese

Pediatrics international, 2005-04, Vol.47 (2), p.137-141

2005

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Neonatal hyperbilirubinemia and a common mutation of the bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese

Journal of human genetics, 1999-01, Vol.44 (1), p.22-25

1999

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Proton NMR study of pure liquid crystal exhibiting re-entrant phase transition

Solid state communications, 1984-01, Vol.49 (7), p.675-678

1984

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Congenital Central Hypoventilation Syndrome: A Novel Mutation of the RET Gene in an Isolated Case

The Tohoku Journal of Experimental Medicine, 2002, Vol.196(4), pp.241-246

2002

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Cytogenetic studies of hynobiidae (Urodela): XVIII. A ZZ/ZW sex-determining mechanism in a hynobiid salamander species, Hynobius tokyoensis Tago: Vertebrate Sex Chromosomes

Cytogenetic and genome research, 2003, Vol.99 (1-4), p.194-199

2003

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Mutation analysis of phenylketonuria in Yamagata prefecture, Japan

Pediatrics international, 2001-02, Vol.43 (1), p.1-3

2001

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Tendon rupture in patients on chronic dialysis

The Japanese Journal of Nephrology, 1986, Vol.28(4), pp.455-460

1986

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Urinary protein analysis and kidney function, with special reference to proteinuria in kidney tubular disorders

Nihon rinshō, 1976-09, Vol.34 (9), p.2857

1976

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Social rehabilitation of patients with kidney diseases and its problem--adult nephrotic syndrome

Nihon rinshō, 1975-12, Vol.33 (12), p.3492

1975

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Digestion and absorption of amino acids and lipids observed in portal venous blood

Shujutsu. Operation, 1970-02, Vol.24 (2), p.206

1970

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Effects of Environmental Factors on Accumulation of CNP in Isaza(Chaenogobius isaza), a Freshwater Fish Living in Lake Biwa

Rikusuigaku zasshi, 1994, Vol.55 (3), p.223-228

1994

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The influence of temperature on the humidity sensitive characteristics of humidity sensitive polymers

Kōbunshi ronbunshū (Tokyo), 1989, Vol.46 (8), p.499-506

1989

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HUMAN AND ANIMAL STUDIES ON PHARMACOKINETICS OF NORFLOXACIN IN RENAL FAILURE

The Japanese Journal of Antibiotics, 1986/10/25, Vol.39(10), pp.2643-2650

1986

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New form of platyspondylic lethal chondrodysplasia

American journal of medical genetics, 1996-12, Vol.66 (4), p.464-467

1996

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Sanitation investments in Ghana: An ethnographic investigation of the role of tenure security, land ownership and livelihoods

BMC public health, 2016-07, Vol.16 (1), p.594-594, Article 594

2016

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A systematic review of diagnostic methods to differentiate acute lung injury/acute respiratory distress syndrome from cardiogenic pulmonary edema

Critical care (London, England), 2017-08, Vol.21 (1), p.228-228, Article 228

2017

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Demographics of tonsillar hypertrophy among sickle cell disease patients in calabar

Bacterial Profile, Susceptibility Patterns, and Factors Associated with Culture-Positive Sputum Among HIV Patients Presenting with a Cough in Northern Uganda

Increased Incidence of Late-Onset Circulatory Collapse after Changing Clinical Practice: A Retrospective Investigation of Causative Factors

Molecular analysis of congenital central hypoventilation syndrome

Cytogenetic studies of Hynobiidae (Urodela)

Neonatal hyperbilirubinemia and mutation of the bilirubin uridine diphosphate‐glucuronosyltransferase gene: a common missense mutation among Japanese, Koreans and Chinese

Cytogenetic studies of Hynobiidae (Urodela)XVIII. A ZZ/ZW sex-determining mechanism in a hynobiid salamander species, Hynobius tokyoensis Tago

Intermittent jaundice in patients with acute leukaemia: A common mutation of the bilirubin uridine‐diphosphate glucuronosyltransferase gene among Asians

Neonatal hyperbilirubinemia in Japanese neonates: Analysis of the heme oxygenase-1 gene and fetal hemoglobin composition in cord blood

Neonatal hyperbilirubinemia and the bilirubin uridine diphosphate-glucuronosyltransferase gene: The common −3263T > G mutation of phenobarbital response enhancer module is not associated with the neonatal hyperbilirubinemia in Japanese

Neonatal hyperbilirubinemia and a common mutation of the bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese

Proton NMR study of pure liquid crystal exhibiting re-entrant phase transition

Congenital Central Hypoventilation Syndrome: A Novel Mutation of the RET Gene in an Isolated Case

Cytogenetic studies of hynobiidae (Urodela): XVIII. A ZZ/ZW sex-determining mechanism in a hynobiid salamander species, Hynobius tokyoensis Tago: Vertebrate Sex Chromosomes

Mutation analysis of phenylketonuria in Yamagata prefecture, Japan

Tendon rupture in patients on chronic dialysis

Urinary protein analysis and kidney function, with special reference to proteinuria in kidney tubular disorders

Social rehabilitation of patients with kidney diseases and its problem--adult nephrotic syndrome

Digestion and absorption of amino acids and lipids observed in portal venous blood

Effects of Environmental Factors on Accumulation of CNP in Isaza(Chaenogobius isaza), a Freshwater Fish Living in Lake Biwa

The influence of temperature on the humidity sensitive characteristics of humidity sensitive polymers

HUMAN AND ANIMAL STUDIES ON PHARMACOKINETICS OF NORFLOXACIN IN RENAL FAILURE

New form of platyspondylic lethal chondrodysplasia

Sanitation investments in Ghana: An ethnographic investigation of the role of tenure security, land ownership and livelihoods

A systematic review of diagnostic methods to differentiate acute lung injury/acute respiratory distress syndrome from cardiogenic pulmonary edema

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