sulfobromophthalein has been researched along with Hyperbilirubinemia, Hereditary in 66 studies
Sulfobromophthalein: A phenolphthalein that is used as a diagnostic aid in hepatic function determination.
Hyperbilirubinemia, Hereditary: Inborn errors of bilirubin metabolism resulting in excessive amounts of bilirubin in the circulating blood, either because of increased bilirubin production or because of delayed clearance of bilirubin from the blood.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Three cases of non-haemolytic constitutional icterus with prevalently conjugated bilirubin have been studied: one case of Dubin-Johnson syndrome and two cases of Rotor's syndrome." | 7.66 | [Constitutional hyperbilirubinemia and mixed bilirubin. Clinical and functional study]. ( Anti, M; De Simone, F; De Vitis, I; Fedeli, G; Miggiano, G; Rapaccini, GL, 1980) |
| "Three cases of non-haemolytic constitutional icterus with prevalently conjugated bilirubin have been studied: one case of Dubin-Johnson syndrome and two cases of Rotor's syndrome." | 3.66 | [Constitutional hyperbilirubinemia and mixed bilirubin. Clinical and functional study]. ( Anti, M; De Simone, F; De Vitis, I; Fedeli, G; Miggiano, G; Rapaccini, GL, 1980) |
| "Sulfobromophthalein (BSP) and its three major forms of conjugates were determined in bile or duodenal aspitate, plasma and urine following intravenous administration of free BSP and synthetic BSP-glutathione (BSP-GSH) in five patients with the Dubin-Johnson syndrome and two patients with the Rotor syndrome, using alumina column chromatography." | 3.65 | Biliary excretion of conjugated sulfobromophthalein (BSP) in constitutional conjugated hyperbilirubinemias. ( Abe, H; Okuda, K, 1975) |
| "Gilbert's syndrome is typically associated with a deficiency in hepatic bilirubin UDP-glucuronosyltransferase activity (B-GTA)." | 2.36 | New insights into the classification and mechanisms of hereditary, chronic, non-haemolytic hyperbilirubinaemias. ( Berthelot, P; Dhumeaux, D, 1978) |
| "Future studies of Gilbert's syndrome must take into account the existence of these subgroups, since they may have different underlying pathogenetic mechanisms." | 2.35 | Abnormal hepatic transport of indocyanine green in Gilbert's syndrome. ( Berk, PD; Martin, JF; Scharschmidt, BF; Vergalla, J; Vierling, JM; Waggoner, JG; Wolkoff, AW, 1976) |
| "The cause of Rotor syndrome (RS), a rare-familial conjugated hyperbilirubinaemia with normal liver histology, is unclear." | 1.34 | Rotor-type hyperbilirubinaemia has no defect in the canalicular bilirubin export pump. ( Cebecauerová, D; Hartmannová, H; Hozák, P; Hrebícek, M; Ivánek, R; Jirásek, T; Jirsa, M; Kmoch, S; Mikulecký, M; Nosková, L; Stránecký, V; Subhanová, I; Vítek, L, 2007) |
| "It is concluded that in Gilbert's syndrome two weeks of treatment with cimetidine had no effect on liver blood flow or on conjugation mechanisms which were independent of cytochrome P450." | 1.27 | Effect of cimetidine on the metabolism of cholephilic dyes in Gilbert's syndrome. ( Deres, M; Kutz, K, 1984) |
| "The recognition that Gilbert's syndrome is a quite heterogeneous entity will allow a better understanding of the mode of inheritance of this disorder; its relationship to Crigler-Najjar type II disease also awaits further definition." | 1.27 | Familial unconjugated hyperbilirubinemia syndromes. ( Reichen, J, 1983) |
| "The 13 patients with Gilbert's syndrome could be divided into three groups according to their BSP disappearance curves: in 7 the curves were normal; another 3 patients the disappearance rate of BSP was normal at the beginning, but became abnormally low later on; and in the last 3 patients, an abnormal BSP disappearance rate was observed during the whole experiment." | 1.27 | Bromsulfophthalein clearance and aminopyrine test in patients with Gilbert's syndrome. ( Bar-Meir, S; Bar-Tal, L; Papa, MZ; Peled, Y, 1986) |
| "This effect is higher in Gilbert's syndrome (GS) and this test has been used in the diagnosis of the syndrome." | 1.27 | Sex differences of nicotinate-induced hyperbilirubinemia in Gilbert's syndrome. Implication of bilitranslocase function. ( Baldini, G; Gentile, S; Lunazzi, G; Sottocasa, GL; Tiribelli, C, 1985) |
| "in the Rotor syndrome 131I-BSP uptake was delayed and liver clearance prolonged; 4." | 1.26 | [Contribution of sequential scintigraphy with 131I-BSP to the differential diagnosis of jaundice (author's transl)]. ( Cotul, S; Dumitrascu, D; Szántai, J; Tamás, S; Tapalaga, D, 1981) |
| "mumol/l in 14 patients with Gilbert's syndrome." | 1.25 | [Diagnostic significance of serum bile acids]. ( Paumgartner, G; Preisig, R; Schwarz, HP, 1975) |
| "Patients with Gilbert's syndrome suffer from an abnormality which makes them jaundiced from time to time." | 1.25 | Gilbert's syndrome in patients with gallbladder stones. ( Peel, AL; Ritchie, HD, 1974) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 56 (84.85) | 18.7374 |
| 1990's | 9 (13.64) | 18.2507 |
| 2000's | 1 (1.52) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| MARTIUS, G | 1 |
| HUBER, W | 1 |
| Hrebícek, M | 1 |
| Jirásek, T | 1 |
| Hartmannová, H | 1 |
| Nosková, L | 1 |
| Stránecký, V | 1 |
| Ivánek, R | 1 |
| Kmoch, S | 1 |
| Cebecauerová, D | 1 |
| Vítek, L | 1 |
| Mikulecký, M | 1 |
| Subhanová, I | 1 |
| Hozák, P | 1 |
| Jirsa, M | 1 |
| Wolkoff, AW | 3 |
| Shiota, T | 1 |
| Watanabe, A | 1 |
| Itoshima, T | 1 |
| Yamamoto, H | 1 |
| Takahashi, K | 1 |
| Nagashima, H | 1 |
| Kutz, K | 2 |
| Deres, M | 1 |
| Kandler, H | 1 |
| Gugler, R | 1 |
| Fevery, J | 1 |
| Reichen, J | 1 |
| Galli, G | 1 |
| Focacci, C | 1 |
| Maini, CL | 1 |
| Salvatori, M | 1 |
| Troncone, L | 1 |
| Fedeli, GL | 1 |
| Rapaccini, GL | 2 |
| Okumura, H | 1 |
| Fukuda, N | 1 |
| Aramaki, T | 1 |
| Katsuta, Y | 1 |
| Satomura, K | 1 |
| Sato, T | 1 |
| Yano, T | 1 |
| Tapalaga, D | 1 |
| Szántai, J | 1 |
| Cotul, S | 1 |
| Tamás, S | 1 |
| Dumitrascu, D | 1 |
| Anti, M | 1 |
| Miggiano, G | 1 |
| De Vitis, I | 1 |
| De Simone, F | 1 |
| Fedeli, G | 1 |
| Nambu, M | 2 |
| Namihisa, T | 3 |
| Hamaguchi, H | 1 |
| Yamaguchi, Y | 1 |
| Goto, M | 1 |
| Misumi, M | 1 |
| Hisama, N | 1 |
| Miyanari, N | 1 |
| Mori, K | 1 |
| Ogawa, M | 1 |
| Shimamura, H | 1 |
| Suzuki, H | 1 |
| Tagaya, O | 4 |
| Horie, T | 2 |
| Sugiyama, Y | 1 |
| Berthelot, P | 1 |
| Dhumeaux, D | 1 |
| Breckenridge, A | 1 |
| Knoflach, P | 1 |
| Horak, W | 1 |
| Kerstan, E | 1 |
| Thaler, H | 1 |
| Kawasaki, H | 2 |
| Kimura, N | 1 |
| Irisa, T | 2 |
| Hirayama, C | 2 |
| Hirata, H | 1 |
| Kamoi, I | 1 |
| Matsuura, K | 1 |
| Röllinghoff, W | 1 |
| Preisig, R | 2 |
| Okolicsanyi, L | 1 |
| Ghidini, O | 1 |
| Orlando, R | 1 |
| Cortelazzo, S | 1 |
| Benedetti, G | 1 |
| Naccarato, R | 1 |
| Manitto, P | 1 |
| Martin, JF | 1 |
| Vierling, JM | 1 |
| Scharschmidt, BF | 2 |
| Vergalla, J | 1 |
| Waggoner, JG | 3 |
| Berk, PD | 3 |
| Wolpert, E | 1 |
| Pascasio, FM | 1 |
| Arias, IM | 2 |
| Solís Herruzo, JA | 1 |
| Schwarz, HP | 1 |
| Paumgartner, G | 1 |
| Abe, H | 1 |
| Okuda, K | 1 |
| Cartei, G | 1 |
| Chisesi, T | 1 |
| Cazzavillian, M | 1 |
| Barbui, T | 1 |
| Battista, R | 1 |
| Dini, E | 1 |
| Hosokawa, S | 1 |
| Mikami, T | 2 |
| Nozaki, Y | 1 |
| Kawaguchi, A | 1 |
| Yamatsu, K | 1 |
| Shamoto, M | 1 |
| Takikawa, H | 1 |
| Sano, N | 1 |
| Narita, T | 1 |
| Uchida, Y | 1 |
| Yamanaka, M | 1 |
| Kurisu, H | 1 |
| Kamisaka, K | 1 |
| Koyo, T | 1 |
| Yamasuge, S | 1 |
| Igarashi, H | 1 |
| Maezawa, H | 1 |
| Uesugi, T | 1 |
| Kitamura, T | 1 |
| Jansen, P | 1 |
| Hardenbrook, C | 1 |
| Kamimoto, Y | 1 |
| Gatmaitan, Z | 1 |
| Gentile, S | 3 |
| Persico, M | 2 |
| Tiribelli, C | 2 |
| Kuipers, F | 1 |
| Radominska, A | 1 |
| Zimniak, P | 1 |
| Little, JM | 1 |
| Havinga, R | 1 |
| Vonk, RJ | 1 |
| Lester, R | 1 |
| Adachi, Y | 1 |
| Yamamoto, T | 1 |
| Bar-Meir, S | 1 |
| Bar-Tal, L | 1 |
| Papa, MZ | 1 |
| Peled, Y | 1 |
| Del Vecchio Blanco, C | 1 |
| Marmo, R | 1 |
| Coltorti, M | 1 |
| Baldini, G | 1 |
| Lunazzi, G | 1 |
| Sottocasa, GL | 1 |
| Maxwell, JD | 1 |
| Hunter, J | 1 |
| Stewart, DA | 1 |
| Carrella, M | 1 |
| Williams, R | 1 |
| Peel, AL | 1 |
| Ritchie, HD | 1 |
| Iio, M | 2 |
| Colón, AR | 1 |
| Sandberg, DH | 1 |
| Feldmann, G | 1 |
| Molas, G | 1 |
| Groussard, O | 1 |
| Domart-Oudea, MC | 1 |
| Brügmann, E | 2 |
| Blaschke, TF | 2 |
| Guyther, JR | 1 |
| Vergalla, JM | 1 |
| Kotlarek-Haus, S | 1 |
| Nowicka, J | 1 |
| Szczeklik, A | 1 |
| Smakowska, E | 1 |
| Kuroda, H | 1 |
| Hisauchi, T | 1 |
| Kobayashi, N | 1 |
| Nanbu, K | 1 |
| Bircher, J | 1 |
| Egger, G | 1 |
| Sommer, W | 1 |
| Lull, RJ | 1 |
| Sievers, P | 1 |
| Gentilini, P | 2 |
| Cornelius, CE | 2 |
| Grodsky, GM | 1 |
| Kolb, HJ | 1 |
| Fanska, RE | 1 |
| Nemechek, C | 1 |
| Yamada, H | 1 |
| Kameda, H | 1 |
| Ueda, H | 1 |
| Sakai, K | 1 |
| Amagase, H | 1 |
| Koizumi, T | 1 |
| Kamata, T | 1 |
| Takino, T | 1 |
| Raymond, GD | 1 |
| Galambos, JT | 1 |
| Laudano, OM | 1 |
| Iglesias, O | 1 |
| Gomez, E | 1 |
| Ito, K | 1 |
| Nakagawa, J | 1 |
| Nakano, H | 1 |
| Tamai, Y | 1 |
| Maeda, K | 1 |
| Orellana Alcalde, JM | 1 |
| Lemus, J | 1 |
| Pablo Dominguez, J | 1 |
| Lücking, T | 1 |
| Kollmann, W | 1 |
| Seseke, G | 1 |
| Surrenti, C | 1 |
| Candidi Tommasi, A | 1 |
| Camilloni, R | 1 |
| Gronwall, RR | 1 |
| Kennelly, BM | 1 |
| Kavin, H | 1 |
| Saunders, SJ | 1 |
7 reviews available for sulfobromophthalein and Hyperbilirubinemia, Hereditary
| Article | Year |
|---|---|
Inheritable disorders manifested by conjugated hyperbilirubinemia.
Topics: Adolescent; Adult; Bile Acids and Salts; Cholecystography; Cholestasis, Intrahepatic; Coproporphyrin | 1983 |
Hepatic transport and metabolism of various organic anions in patients with congenital non-hemolytic hyperbilirubinemia, including constitutional indocyanine green excretory defect.
Topics: Bilirubin; Biological Transport; Female; Humans; Hyperbilirubinemia, Hereditary; Indocyanine Green; | 1994 |
New insights into the classification and mechanisms of hereditary, chronic, non-haemolytic hyperbilirubinaemias.
Topics: Bilirubin; Chronic Disease; Coproporphyrins; Crigler-Najjar Syndrome; Female; Gilbert Disease; Glucu | 1978 |
Clinical implications of enzyme induction.
Topics: Animals; Barbiturates; Bile; Bilirubin; Digitoxin; Enzyme Induction; gamma-Glutamyltransferase; Gluc | 1975 |
Abnormal hepatic transport of indocyanine green in Gilbert's syndrome.
Topics: Adolescent; Adult; Aged; Bilirubin; Biological Transport; Child; Female; Gilbert Disease; Glucuronos | 1976 |
[Advances in the differential diagnosis of cholestasis--nuclear medicine].
Topics: Cholestasis; Diagnosis, Differential; Humans; Hyperbilirubinemia; Hyperbilirubinemia, Hereditary; Ja | 1972 |
Presently recognized forms of inherited jaundice in infancy. A summary and review.
Topics: Bilirubin; Biological Transport; Cholestasis; Diagnosis, Differential; Feces; Galactosemias; Hepatit | 1973 |
59 other studies available for sulfobromophthalein and Hyperbilirubinemia, Hereditary
| Article | Year |
|---|---|
[BROMSULPHALEIN CLEARANCE AND BILIRUBIN DETERMINATIONS IN NEWBORN INFANTS].
Topics: Bilirubin; Female; Humans; Hyperbilirubinemia; Hyperbilirubinemia, Hereditary; Infant; Infant, Newbo | 1964 |
Rotor-type hyperbilirubinaemia has no defect in the canalicular bilirubin export pump.
Topics: Aged; DNA Mutational Analysis; Family Health; Humans; Hyperbilirubinemia, Hereditary; Jaundice, Chro | 2007 |
Two cases of constitutional unconjugated hyperbilirubinemia with marked retention of indocyanine green.
Topics: Adult; Gilbert Disease; Glucuronosyltransferase; Humans; Hyperbilirubinemia, Hereditary; Indocyanine | 1984 |
Effect of cimetidine on the metabolism of cholephilic dyes in Gilbert's syndrome.
Topics: Adolescent; Adult; Alanine Transaminase; Alkaline Phosphatase; Aspartate Aminotransferases; Bile; Bi | 1984 |
Effect of clofibrate on the metabolism of bilirubin, bromosulphophthalein and indocyanine green and on the biliary lipid composition in Gilbert's syndrome.
Topics: Adult; Bile; Bilirubin; Clofibrate; Female; Gilbert Disease; Humans; Hyperbilirubinemia, Hereditary; | 1984 |
Familial unconjugated hyperbilirubinemia syndromes.
Topics: Animals; Bile Acids and Salts; Bilirubin; Crigler-Najjar Syndrome; Diagnosis, Differential; Disease | 1983 |
The hepatic excretion of 131I-rose bengal and 99mTc-IDA derivatives in Rotor's syndrome.
Topics: Adult; Bilirubin; Humans; Hyperbilirubinemia, Hereditary; Imino Acids; Iodine Radioisotopes; Liver; | 1982 |
Rotor's syndrome: a study on variations in pigment metabolism with age.
Topics: Adolescent; Adult; Aging; Bilirubin; Female; Humans; Hyperbilirubinemia, Hereditary; Male; Sulfobrom | 1982 |
[Contribution of sequential scintigraphy with 131I-BSP to the differential diagnosis of jaundice (author's transl)].
Topics: Diagnosis, Differential; Gilbert Disease; Humans; Hyperbilirubinemia, Hereditary; Iodine Radioisotop | 1981 |
[Constitutional hyperbilirubinemia and mixed bilirubin. Clinical and functional study].
Topics: Adult; Bilirubin; Female; Humans; Hyperbilirubinemia; Hyperbilirubinemia, Hereditary; Jaundice, Chro | 1980 |
Hepatic biliary transport after hepatocyte transplantation in Eizai hyperbilirubinemic rats.
Topics: Animals; Bile; Bile Acids and Salts; Bilirubin; Biological Transport; Cell Transplantation; Hepatect | 1994 |
Hepatic transport of serum bilirubin, bromsulfophthalein, and indocyanine green in patients with congenital non-hemolytic hyperbilirubinemia and patients with constitutional indocyanine green excretory defect.
Topics: Adult; Bilirubin; Biological Transport; Coloring Agents; Diagnosis, Differential; Female; Humans; Hy | 1996 |
Biliary excretion of glycyrrhizin in rats: kinetic basis for multiplicity in bile canalicular transport of organic anions.
Topics: Animals; Bile; Bile Canaliculi; Biological Transport; Glycyrrhetinic Acid; Glycyrrhizic Acid; Hyperb | 1996 |
[Benign chronic conjugated hyperbilirubinaemia: rotor syndrome or hepatic storage impairment?].
Topics: Diagnosis, Differential; Female; Humans; Hyperbilirubinemia, Hereditary; Jaundice, Chronic Idiopathi | 1979 |
Dye clearance studies in Rotor's syndrome.
Topics: Adolescent; Adult; Aged; Bilirubin; Female; Humans; Hyperbilirubinemia, Hereditary; Indocyanine Gree | 1979 |
[Scintigraphic diagnosis of constitutional jaundice using 131I-B.S.P. (author's transl)].
Topics: Adolescent; Adult; Gilbert Disease; Humans; Hyperbilirubinemia, Hereditary; Iodine Radioisotopes; Ja | 1978 |
[Recent advances in pathogenesis and diagnosis of constitutional hepatic dysfunction (Gilbert's syndrome) (author's transl)].
Topics: Adult; Bilirubin; Diagnosis, Differential; Humans; Hyperbilirubinemia, Hereditary; Indocyanine Green | 1978 |
An evaluation of bilirubin kinetics with respect to the diagnosis of Gilbert's syndrome.
Topics: Adult; Bilirubin; Biological Transport; Female; Gilbert Disease; Humans; Hyperbilirubinemia, Heredit | 1978 |
Abnormal sulfobromophthalein metabolism in Rotor's syndrome and obligate heterozygotes.
Topics: Chromatography, Paper; Coproporphyrins; Female; Heterozygote; Humans; Hyperbilirubinemia, Hereditary | 1977 |
[Kinetics of bromsulphalein in the non congujate hyperbilirubinemias].
Topics: Drug Evaluation; Gilbert Disease; Humans; Hyperbilirubinemia, Hereditary; Kinetics; Liver; Liver Fun | 1975 |
[Diagnostic significance of serum bile acids].
Topics: Adolescent; Adult; Alkaline Phosphatase; Aspartate Aminotransferases; Bile Acids and Salts; Bilirubi | 1975 |
Biliary excretion of conjugated sulfobromophthalein (BSP) in constitutional conjugated hyperbilirubinemias.
Topics: Adolescent; Adult; Bile; Female; Glutathione; Humans; Hyperbilirubinemia, Hereditary; Jaundice, Chro | 1975 |
[Bromsulphalein clearance and hyperbilirubinemia in Gilbert's syndrome].
Topics: Biliary Tract; Gilbert Disease; Humans; Hyperbilirubinemia; Hyperbilirubinemia, Hereditary; Liver; S | 1975 |
A new rat mutant with chronic conjugated hyperbilirubinemia and renal glomerular lesions.
Topics: Animals; Bilirubin; Chronic Disease; Disease Models, Animal; Female; Glomerulonephritis; Hyperbiliru | 1992 |
Biliary excretion of bile acid conjugates in a hyperbilirubinemic mutant Sprague-Dawley rat.
Topics: Animals; Bile; Bile Acids and Salts; Chenodeoxycholic Acid; Chromatography, Gel; Chromatography, Thi | 1991 |
Organic anion transport study in mutant rats with autosomal recessive conjugated hyperbilirubinemia.
Topics: Animals; Bile; Bile Acids and Salts; Bilirubin; Hyperbilirubinemia, Hereditary; Indocyanine Green; R | 1991 |
Defective ATP-dependent bile canalicular transport of organic anions in mutant (TR-) rats with conjugated hyperbilirubinemia.
Topics: Adenosine Triphosphate; Animals; Anions; Bile; Bile Canaliculi; Bile Ducts, Intrahepatic; Biological | 1990 |
Abnormal hepatic uptake of low doses of sulfobromophthalein in Gilbert's syndrome: the role of reduced affinity of the plasma membrane carrier of organic anions.
Topics: Adolescent; Adult; Anions; Carrier Proteins; Cell Membrane; Female; Gilbert Disease; Humans; Hyperbi | 1990 |
Defective biliary secretion of bile acid 3-O-glucuronides in rats with hereditary conjugated hyperbilirubinemia.
Topics: Androstanols; Animals; Bile Acids and Salts; Glucuronates; Glucuronosyltransferase; Hyperbilirubinem | 1989 |
Partial defect in hepatic glutathione S-transferase activity in a case of Rotor's syndrome.
Topics: Adolescent; Adult; Aged; Cholelithiasis; Dinitrochlorobenzene; Glucosyltransferases; Glucuronosyltra | 1987 |
Bromsulfophthalein clearance and aminopyrine test in patients with Gilbert's syndrome.
Topics: Adolescent; Adult; Aged; Aminopyrine; Breath Tests; Female; Gilbert Disease; Humans; Hyperbilirubine | 1986 |
Familial clustering of heterogeneous chronic unconjugated hyperbilirubinemia.
Topics: Adult; Child; Chronic Disease; Female; Half-Life; Humans; Hyperbilirubinemia, Hereditary; Male; Midd | 1986 |
Sex differences of nicotinate-induced hyperbilirubinemia in Gilbert's syndrome. Implication of bilitranslocase function.
Topics: Adolescent; Adult; Animals; Bilirubin; Binding, Competitive; Ceruloplasmin; Female; Gilbert Disease; | 1985 |
Effect of phenobarbitone on bile flow and bilirubin metabolism in man and the rat.
Topics: Adipates; Animals; Bile; Bilirubin; Body Weight; Cytochrome P-450 Enzyme System; Enzyme Induction; G | 1973 |
Gilbert's syndrome in patients with gallbladder stones.
Topics: Adult; Alkaline Phosphatase; Bilirubin; Cell Survival; Cholangiography; Cholecystectomy; Cholecystog | 1974 |
[Liver ultrastructure in idiopathic chronic jaundice].
Topics: Adult; Bilirubin; Humans; Hyperbilirubinemia, Hereditary; Jaundice, Chronic Idiopathic; Liver; Male; | 1972 |
[Different elimination velocity of indocyanine green in liver diseases of various severity].
Topics: Chronic Disease; Fatty Liver; Hepatitis; Humans; Hyperbilirubinemia, Hereditary; Indocyanine Green; | 1973 |
Crigler-Najjar syndrome: an unusual course with development of neurologic damage at age eighteen.
Topics: Adolescent; Alkaline Phosphatase; Bilirubin; Brain Damage, Chronic; Brain Diseases; Carbon Monoxide; | 1974 |
[Diagnostic difficulties in cases of congenital hyperbilirubinemia].
Topics: Adult; Diagnosis, Differential; Female; Humans; Hyperbilirubinemia, Hereditary; Jaundice, Chronic Id | 1974 |
[Electron microscopic study of constitutional ICG excretory defect].
Topics: Adult; Female; Humans; Hyperbilirubinemia, Hereditary; Indocyanine Green; Liver; Male; Microscopy, E | 1974 |
[Diagnosis as therapy--enlightment of patients with constitutional hyperbilirubinemia (Gilbert-Meulengracht)].
Topics: Adolescent; Adult; Bilirubin; Chromium Isotopes; Erythrocytes; Female; Galactose; Health Education; | 1972 |
Defective bromosulfophthalein clearance in patients with constitutional hepatic dysfunction (Gilbert's syndrome).
Topics: Adolescent; Adult; Biopsy; Chromium Isotopes; Erythrocytes; Female; Hemolysis; Humans; Hyperbilirubi | 1972 |
Further observation on 131 I-rose bengal clearance in Gilbert's disease.
Topics: Humans; Hyperbilirubinemia, Hereditary; Iodine Radioisotopes; Liver; Liver Function Tests; Rose Beng | 1971 |
[Comparative dye loading tests using indocyanine green and bromsulphalein in Gilbert's constitutional idiopathic hyperbilirubinemia].
Topics: Humans; Hyperbilirubinemia, Hereditary; Indocyanine Green; Liver Diseases; Liver Function Tests; Met | 1971 |
[Diagnostic significance of bilirubinemia].
Topics: Adolescent; Adult; Alanine Transaminase; Aspartate Aminotransferases; Bilirubin; Female; Hepatitis; | 1971 |
Organic anion transport in mutant sheep with congenital hyperbilirubinemia.
Topics: Animals; Bilirubin; Biological Transport; Disease Models, Animal; Gallbladder; Humans; Hyperbilirubi | 1969 |
Effect of age of rat on development of hepatic carriers for bilirubin: a possible explanation for physiologic jaundice and hyperbilirubinemia in the newborn.
Topics: Age Factors; Animals; Bilirubin; Chromatography, Gel; Humans; Hydrogen-Ion Concentration; Hyperbilir | 1970 |
Diagnosis and differentiation of constitutional hyperbilirubinemias using sequential scanning with 131-I-BSP (monoiodide).
Topics: Adult; Humans; Hyperbilirubinemia, Hereditary; Iodine Radioisotopes; Liver Function Tests; Male; Mid | 1971 |
[Congenital non-hemolytic and non-conjugating-type hyperbilirubinemia].
Topics: Adolescent; Bilirubin; Female; Humans; Hyperbilirubinemia, Hereditary; Indocyanine Green; Iodine Iso | 1971 |
[Alternate hyperbilirubinemia].
Topics: Adult; Humans; Hyperbilirubinemia, Hereditary; Liver Function Tests; Male; Menthol; Osmotic Fragilit | 1971 |
[Rotor-type hyperbilirubinemia].
Topics: Adult; Cytoplasmic Granules; Humans; Hyperbilirubinemia, Hereditary; Indocyanine Green; Liver; Male; | 1971 |
Hepatic storage and excretion of bilirubin in man.
Topics: Adolescent; Adult; Anemia, Hemolytic; Animals; Bilirubin; Dogs; Hepatitis; Humans; Hyperbilirubinemi | 1971 |
[Total free and conjugated bromsulphalein clearance, in Dubin-Johnson and Gilbert's syndromes].
Topics: Adult; Female; Humans; Hyperbilirubinemia, Hereditary; Jaundice, Chronic Idiopathic; Male; Sulfobrom | 1967 |
[Interpretation of bromsulphalein (BSP) value in liver diseases--with special reference to the analytical result of BSP metabolism].
Topics: Humans; Hyperbilirubinemia, Hereditary; Liver Diseases; Liver Function Tests; Sulfobromophthalein | 1967 |
[Histological study (light microscopy) of recurrent jaundice due to familial defect of bilirubin excretion without liver involvement].
Topics: Chronic Disease; Ethanol; Female; Humans; Hyperbilirubinemia, Hereditary; Jaundice; Middle Aged; Nov | 1968 |
[Chronic non-hemolytic hyperbilirubinemia with elevated bound bilirubins (Rotor syndrome). Report of 2 new cases].
Topics: Biopsy; Child; Child, Preschool; Chronic Disease; Female; Humans; Hyperbilirubinemia, Hereditary; Li | 1968 |
[Studies of the interference between bilirubin metabolism and BSP metabolism in humans. Preliminary results].
Topics: Bilirubin; Fatty Liver; Hepatitis; Humans; Hyperbilirubinemia; Hyperbilirubinemia, Hereditary; Liver | 1968 |
Congenital photosensitivity and hyperbilirubinemia in Southdown sheep in the United States.
Topics: Animals; Bilirubin; Hyperbilirubinemia, Hereditary; Indocyanine Green; Iodine Radioisotopes; Liver F | 1968 |
Observations on a family with chronic hyperbilirubinaemia.
Topics: Adult; Cholecystography; Female; Humans; Hyperbilirubinemia, Hereditary; Liver Function Tests; Middl | 1969 |