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nadp and Infant, Newborn, Diseases

nadp has been researched along with Infant, Newborn, Diseases in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19905 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
KOSOY, MH; NAIMAN, JL1
FISCHER, D; HARTLEYB, H; HEIDT, P; LAUSECKER, C; LOHR, GW1
Hsia, DY; Nelson, K1
Good, RA; Holmes, B; Malawista, SE; Nelson, DL; Park, BH; Quie, PG1
Bellanti, JA; Cantz, BE; Schlegel, RJ1

Other Studies

5 other study(ies) available for nadp and Infant, Newborn, Diseases

ArticleYear
RED CELL GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY--A NEWLY RECOGNIZED CAUSE OF NEONATAL JAUNDICE AND KERNICTERUS IN CANADA.
    Canadian Medical Association journal, 1964, Dec-12, Volume: 91

    Topics: Analgesics; Analgesics, Non-Narcotic; Antimalarials; Antipyretics; Asian People; Biochemical Phenomena; Biochemistry; Canada; Drug Therapy; Erythrocytes; Ethnology; Exchange Transfusion, Whole Blood; Genetics, Medical; Glucosephosphate Dehydrogenase Deficiency; Glucosephosphates; Hemolysis; Humans; Hyperbilirubinemia; Infant, Newborn; Infant, Newborn, Diseases; Jaundice; Jaundice, Neonatal; Kernicterus; Male; Methemoglobin; NADP; Naphthalenes; Nitrofurans; Sex; Statistics as Topic; Sulfanilamide; Sulfanilamides; Sulfonamides; Toxicology; White People

1964
[A NEW CASE OF RECESSIVE CONGENITAL METHEMOGLOBINEMIA LINKED WITH A DIAPHORASE I DEFICIENCY].
    Archives francaises de pediatrie, 1964, Volume: 21

    Topics: Ascorbic Acid; Cytochrome-B(5) Reductase; Dihydrolipoamide Dehydrogenase; Drug Therapy; Genetics, Medical; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Metabolic Diseases; Methemoglobinemia; Methylene Blue; NAD; NADP

1964
Screening for galactosemia and glucose-6-phosphate dehydrogenase deficiency in newborn infants.
    The Journal of pediatrics, 1967, Volume: 71, Issue:4

    Topics: Clinical Enzyme Tests; Galactosemias; Glucosephosphate Dehydrogenase; Glucosephosphate Dehydrogenase Deficiency; Humans; Infant, Newborn; Infant, Newborn, Diseases; Mass Screening; NADP; Nucleotidyltransferases

1967
Chronic granulomatous disease in females.
    The New England journal of medicine, 1970, Jul-30, Volume: 283, Issue:5

    Topics: Chronic Disease; Erythrocytes; Female; Genes; Glucosephosphate Dehydrogenase; Glutathione; Glutathione Reductase; Granuloma; Humans; Infant, Newborn; Infant, Newborn, Diseases; Infections; Leukocytes; Lymphadenitis; Male; NAD; NADP; Oxidoreductases; Peroxidases; Sex Chromosomes; Sex Factors

1970
Accelerated decay of glucose 6-phosphate dehydrogenase activity in chronic granulomatous disease.
    Pediatric research, 1970, Volume: 4, Issue:5

    Topics: Adult; Child; Child, Preschool; Chronic Disease; Erythrocytes; Genes; Glucosephosphate Dehydrogenase; Granuloma; Hot Temperature; Humans; Immunologic Deficiency Syndromes; Infant, Newborn; Infant, Newborn, Diseases; Infections; Leukocytes; Lymphadenitis; Male; NADP; Phagocytosis; Phosphogluconate Dehydrogenase; Sex Chromosomes; Time Factors

1970