Page last updated: 2024-10-21

1-anilino-8-naphthalenesulfonate and Enlarged Liver

1-anilino-8-naphthalenesulfonate has been researched along with Enlarged Liver in 8 studies

1-anilino-8-naphthalenesulfonate: RN given refers to parent cpd
8-anilinonaphthalene-1-sulfonic acid : A naphthalenesulfonic acid that is naphthalene-1-sulfonic acid substituted by a phenylamino group at position 8.

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19904 (50.00)18.7374
1990's1 (12.50)18.2507
2000's2 (25.00)29.6817
2010's1 (12.50)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Habib, A1
Jain, A1
Singh, B1
Jamshed, N1
Badeloe, S1
van Geel, M1
Nagtzaam, I1
Rubio-Gozalbo, ME1
Oei, RL1
Steijlen, PM1
van Steensel, MA1
Schaub, J1
Janka, GE1
Christomanou, H1
Sandhoff, K1
Permanetter, W1
Hübner, G1
Meister, P1
vom Dahl, S1
Harzer, K1
Rolfs, A1
Albrecht, B1
Niederau, C1
Vogt, C1
van Weely, S1
Aerts, J1
Müller, G1
Häussinger, D1
Du, H1
Heur, M1
Duanmu, M1
Grabowski, GA1
Hui, DY1
Witte, DP1
Mishra, J1
Berdel, D1
Beaudet, AL1
Ferry, GD1
Nichols, BL1
Rosenberg, HS1
Burke, JA1
Schubert, WK1

Other Studies

8 other studies available for 1-anilino-8-naphthalenesulfonate and Enlarged Liver

ArticleYear
H1N1 influenza presenting as severe acute pancreatitis and multiorgan dysfunction.
    The American journal of emergency medicine, 2016, Volume: 34, Issue:9

    Topics: Acute Kidney Injury; Adult; Amylases; Ascites; Blood Urea Nitrogen; Creatinine; Female; Hepatomegaly

2016
Chanarin-Dorfman syndrome caused by a novel splice site mutation in ABHD5.
    The British journal of dermatology, 2008, Volume: 158, Issue:6

    Topics: 1-Acylglycerol-3-Phosphate O-Acyltransferase; Child; Consanguinity; Diagnosis, Differential; Hepatom

2008
Wolman's disease: clinical, biochemical and ultrastructural studies in an unusual case without striking adrenal calcification.
    European journal of pediatrics, 1980, Volume: 135, Issue:1

    Topics: Adrenal Glands; Bone Marrow; Female; Hepatomegaly; Humans; Infant; Leukocytes; Lipase; Lipid Metabol

1980
Hepatosplenomegalic lipidosis: what unless Gaucher? Adult cholesteryl ester storage disease (CESD) with anemia, mesenteric lipodystrophy, increased plasma chitotriosidase activity and a homozygous lysosomal acid lipase -1 exon 8 splice junction mutation.
    Journal of hepatology, 1999, Volume: 31, Issue:4

    Topics: Adult; Anemia; Cholesterol Ester Storage Disease; Diagnosis, Differential; DNA, Recombinant; Exons;

1999
Lysosomal acid lipase-deficient mice: depletion of white and brown fat, severe hepatosplenomegaly, and shortened life span.
    Journal of lipid research, 2001, Volume: 42, Issue:4

    Topics: Adipocytes; Adipose Tissue; Adipose Tissue, Brown; Aging; Animals; Blood Glucose; Cell Differentiati

2001
[A case of hyperlipoproteinaemia of type I (author's transl)].
    Klinische Padiatrie, 1979, Volume: 191, Issue:3

    Topics: Abducens Nerve; Child; Chylomicrons; Hepatomegaly; Humans; Hyperlipidemias; Lipase; Male; Paralysis;

1979
Cholesterol ester storage disease: clinical, biochemical, and pathological studies.
    The Journal of pediatrics, 1977, Volume: 90, Issue:6

    Topics: Child; Cholesterol; Cholesterol Esters; Female; Fibroblasts; Hepatomegaly; Histocytochemistry; Human

1977
Deficient activity of acid lipase in cholesterol-ester storage disease.
    The Journal of laboratory and clinical medicine, 1971, Volume: 78, Issue:6

    Topics: Cholesterol; Esters; Hepatomegaly; Humans; Lipase; Lipid Metabolism, Inborn Errors; Lipidoses; Liver

1971