1-anilino-8-naphthalenesulfonate has been researched along with Syndrome in 65 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.
Syndrome: A characteristic symptom complex.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Our objective was to determine whether fenofibrate modifies the metabolism of nonesterified (free) fatty acids as a component of its triglyceride-lowering action in male patients with the metabolic syndrome." | 9.10 | Free fatty acid metabolism during fenofibrate treatment of the metabolic syndrome. ( Cater, NB; Grundy, SM; Hadizadeh, DR; Meguro, S; Vega, GL, 2003) |
| "In the past 6 years, 11 children on valproic acid have developed pancreatitis in our children's hospital." | 7.72 | Valproic acid-induced pancreatitis in childhood epilepsy: case series and review. ( Berg, M; Breault, R; Sinclair, DB, 2004) |
| "Our objective was to determine whether fenofibrate modifies the metabolism of nonesterified (free) fatty acids as a component of its triglyceride-lowering action in male patients with the metabolic syndrome." | 5.10 | Free fatty acid metabolism during fenofibrate treatment of the metabolic syndrome. ( Cater, NB; Grundy, SM; Hadizadeh, DR; Meguro, S; Vega, GL, 2003) |
| "In the past 6 years, 11 children on valproic acid have developed pancreatitis in our children's hospital." | 3.72 | Valproic acid-induced pancreatitis in childhood epilepsy: case series and review. ( Berg, M; Breault, R; Sinclair, DB, 2004) |
| "Wolman disease is a rare disease caused by the absence of functional liposomal acid lipase due to mutations in LIPA gene." | 3.01 | Wolman disease presenting with hemophagocytic lymphohistiocytosis syndrome and a novel LIPA gene variant: a case report and review of the literature. ( Asna Ashari, K; Azari-Yam, A; Shahrooei, M; Ziaee, V, 2023) |
| "Dorfman-Chanarin syndrome is a rare autosomal recessive inherited lipid storage disease characterized by ichthyosis, leukocyte lipid vacuoles, and involvement of several internal organs." | 1.32 | Truncation of CGI-58 protein causes malformation of lamellar granules resulting in ichthyosis in Dorfman-Chanarin syndrome. ( Akiyama, M; Nomura, Y; Sawamura, D; Shimizu, H; Sugawara, M, 2003) |
| "Fat embolism syndrome is most often seen after fracture of long bones, and immobilization of the fracture site may decrease risk of its development." | 1.26 | Fat embolism syndrome: a puzzling phenomenon. ( Gong, H, 1977) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 19 (29.23) | 18.7374 |
| 1990's | 9 (13.85) | 18.2507 |
| 2000's | 25 (38.46) | 29.6817 |
| 2010's | 10 (15.38) | 24.3611 |
| 2020's | 2 (3.08) | 2.80 |
| Authors | Studies |
|---|---|
| Sofela, J | 1 |
| Hunt, WTN | 1 |
| Chaytor, R | 1 |
| Stephens, M | 1 |
| Sofela, A | 1 |
| Harmse, D | 1 |
| Chave, T | 1 |
| Asna Ashari, K | 1 |
| Azari-Yam, A | 1 |
| Shahrooei, M | 1 |
| Ziaee, V | 1 |
| Gubergrits, NB | 1 |
| Gubska, O | 1 |
| Klochkov, AY | 1 |
| Fomenko, PG | 1 |
| Alianova, TS | 1 |
| Bachmeier, CAE | 1 |
| Morton, A | 1 |
| Yoshizawa, M | 1 |
| Nakamura, M | 1 |
| Farooq, M | 1 |
| Inoue, A | 1 |
| Aoki, J | 1 |
| Shimomura, Y | 1 |
| Yang, BL | 1 |
| Wu, WC | 1 |
| Su, CW | 1 |
| Wu, JC | 1 |
| Yeh, C | 1 |
| Lee, SD | 1 |
| Birtolo, C | 1 |
| Migliori, M | 3 |
| Drewes, AM | 1 |
| Tomassetti, P | 2 |
| Imbrogno, A | 1 |
| Fusaroli, P | 1 |
| Casadei, R | 1 |
| Ricci, C | 1 |
| Stanghellini, V | 1 |
| De Giorgio, R | 1 |
| Gullo, L | 3 |
| Laghi, L | 1 |
| Lucrezio, L | 1 |
| Bianchi, P | 1 |
| Randolph, AE | 1 |
| Mantovani, V | 1 |
| Bastagli, L | 1 |
| Pezzilli, R | 2 |
| Malesci, A | 1 |
| Ghosh, AK | 1 |
| Ramakrishnan, G | 1 |
| Chandramohan, C | 1 |
| Rajasekharan, R | 1 |
| Yamaguchi, T | 2 |
| Osumi, T | 2 |
| Radner, FP | 1 |
| Streith, IE | 1 |
| Schoiswohl, G | 2 |
| Schweiger, M | 2 |
| Kumari, M | 1 |
| Eichmann, TO | 1 |
| Rechberger, G | 1 |
| Koefeler, HC | 1 |
| Eder, S | 1 |
| Schauer, S | 1 |
| Theussl, HC | 1 |
| Preiss-Landl, K | 1 |
| Lass, A | 2 |
| Zimmermann, R | 2 |
| Hoefler, G | 1 |
| Zechner, R | 2 |
| Haemmerle, G | 2 |
| Dereure, O | 1 |
| Riediger, C | 1 |
| Mayr, M | 1 |
| Berger, H | 1 |
| Becker, K | 1 |
| Dobritz, M | 1 |
| Kleeff, J | 1 |
| Friess, H | 1 |
| Ozkok, A | 1 |
| Elcioglu, OC | 1 |
| Cukadar, T | 1 |
| Bakan, A | 1 |
| Sasak, G | 1 |
| Atilgan, KG | 1 |
| Alisir, S | 1 |
| Kanbay, M | 1 |
| Covic, A | 1 |
| Odabas, AR | 1 |
| Catanzaro, R | 1 |
| Italia, A | 1 |
| Konno, M | 1 |
| Ventrucci, M | 1 |
| Barakat, B | 1 |
| Vega, GL | 1 |
| Cater, NB | 1 |
| Hadizadeh, DR | 1 |
| Meguro, S | 1 |
| Grundy, SM | 1 |
| PALAZZUOLI, M | 1 |
| PIAZZESI, W | 1 |
| WUKETICH, S | 1 |
| PAVLIK, F | 1 |
| TINCANI, GP | 1 |
| BALDINI, E | 1 |
| Akiyama, M | 2 |
| Sawamura, D | 2 |
| Nomura, Y | 1 |
| Sugawara, M | 1 |
| Shimizu, H | 2 |
| Srinivasan, R | 1 |
| Hadzić, N | 1 |
| Fischer, J | 5 |
| Knisely, AS | 1 |
| Omatsu, N | 1 |
| Matsushita, S | 1 |
| Morató, A | 1 |
| Martínez-Cabot, A | 1 |
| Escabrós, J | 1 |
| Bujons, J | 1 |
| Messeguer, A | 1 |
| Caux, F | 3 |
| Selma, ZB | 1 |
| Laroche, L | 2 |
| Prud'homme, JF | 2 |
| Sinclair, DB | 1 |
| Berg, M | 1 |
| Breault, R | 1 |
| Schleinitz, N | 1 |
| Sanchez, A | 1 |
| Veit, V | 1 |
| Harle, JR | 1 |
| Pelissier, JF | 1 |
| Pujol, RM | 1 |
| Gilaberte, M | 1 |
| Toll, A | 1 |
| Florensa, L | 1 |
| Lloreta, J | 1 |
| González-Enseñat, MA | 1 |
| Azon, A | 1 |
| Solomon, C | 1 |
| Bernier, L | 1 |
| Germain, L | 1 |
| Dufour, R | 1 |
| Davignon, J | 1 |
| Yen, CL | 1 |
| Farese, RV | 1 |
| Riederer, M | 1 |
| Kienesberger, P | 1 |
| Strauss, JG | 1 |
| Gorkiewicz, G | 1 |
| Demerjian, M | 1 |
| Crumrine, DA | 1 |
| Milstone, LM | 1 |
| Williams, ML | 1 |
| Elias, PM | 1 |
| Ben Selma, Z | 1 |
| Yilmaz, S | 1 |
| Schischmanoff, PO | 1 |
| Blom, A | 1 |
| Ozogul, C | 1 |
| Sakai, K | 1 |
| Ogawa, M | 1 |
| McMillan, JR | 1 |
| Bruno, C | 1 |
| Bertini, E | 1 |
| Di Rocco, M | 1 |
| Cassandrini, D | 1 |
| Ruffa, G | 1 |
| De Toni, T | 1 |
| Seri, M | 1 |
| Spada, M | 1 |
| Li Volti, G | 1 |
| D'Amico, A | 1 |
| Trucco, F | 1 |
| Arca, M | 1 |
| Casali, C | 1 |
| Angelini, C | 1 |
| Dimauro, S | 1 |
| Minetti, C | 1 |
| Badeloe, S | 1 |
| van Geel, M | 1 |
| Nagtzaam, I | 1 |
| Rubio-Gozalbo, ME | 1 |
| Oei, RL | 1 |
| Steijlen, PM | 1 |
| van Steensel, MA | 1 |
| Sachs, EF | 1 |
| Bloch, HM | 1 |
| Milne, FJ | 1 |
| Muller, DP | 1 |
| Stafford, RJ | 1 |
| Grand, RJ | 1 |
| Hill, RE | 1 |
| Durie, PR | 2 |
| Gaskin, KJ | 1 |
| Davidson, GP | 1 |
| Forstner, GG | 1 |
| Schlievert, PM | 1 |
| Osterholm, MT | 1 |
| Kelly, JA | 1 |
| Nishimura, RD | 1 |
| Philippart, M | 1 |
| Durand, P | 1 |
| Borrone, C | 1 |
| Barron, DW | 1 |
| Christomanou, H | 1 |
| Cáp, C | 1 |
| Croft, NM | 1 |
| Marshall, TG | 1 |
| Ferguson, A | 1 |
| Knudsen, P | 1 |
| Eriksson, J | 1 |
| Lahdenperä, S | 1 |
| Kahri, J | 1 |
| Groop, L | 1 |
| Taskinen, MR | 1 |
| Jones, NL | 1 |
| Hofley, PM | 1 |
| Doull, I | 1 |
| Langton-Hewer, S | 1 |
| Hershkovits, BS | 1 |
| Dagan, J | 1 |
| Freier, S | 1 |
| McDonald, MC | 2 |
| Filipe, HM | 1 |
| Thiemermann, C | 2 |
| Mota-Filipe, H | 1 |
| Paul, A | 1 |
| Cuzzocrea, S | 1 |
| Abdelrahman, M | 1 |
| Harwood, S | 1 |
| Plevin, R | 1 |
| Chatterjee, PK | 1 |
| Yaqoob, MM | 1 |
| Lefèvre, C | 1 |
| Jobard, F | 1 |
| Bouadjar, B | 1 |
| Karaduman, A | 1 |
| Heilig, R | 1 |
| Lakhdar, H | 1 |
| Wollenberg, A | 1 |
| Verret, JL | 1 |
| Weissenbach, J | 1 |
| Ozgüc, M | 1 |
| Lathrop, M | 1 |
| Cortner, JA | 1 |
| Coates, PM | 1 |
| Swoboda, E | 1 |
| Schnatz, JD | 1 |
| Schaffner, T | 1 |
| Elner, VM | 1 |
| Bauer, M | 1 |
| Wissler, RW | 1 |
| von Bassewitz, DB | 1 |
| Roggenkamp, K | 1 |
| Strehl, H | 1 |
| Otto, H | 1 |
| Gong, H | 1 |
| Suzuki, Y | 1 |
| Kawai, S | 1 |
| Kobayashi, A | 1 |
| Ohbe, Y | 1 |
| Endo, H | 1 |
| Smirnov, KV | 1 |
| Blomhoff, JP | 1 |
| Lechowski, R | 1 |
| Pisarski, J | 1 |
| Gosławski, J | 1 |
| Lenarcik, M | 1 |
| Brown, WJ | 1 |
| Warfel, J | 1 |
| Greenspan, P | 1 |
| Kyriakides, EC | 1 |
| Paul, B | 1 |
| Balint, JA | 1 |
| Maggi, V | 1 |
| Gahan, PB | 1 |
| Khan, W | 1 |
| Kutty, KM | 1 |
| Rowden, G | 1 |
8 reviews available for 1-anilino-8-naphthalenesulfonate and Syndrome
| Article | Year |
|---|---|
Wolman disease presenting with hemophagocytic lymphohistiocytosis syndrome and a novel LIPA gene variant: a case report and review of the literature.
Topics: Child; Exons; Humans; Infant; Lipase; Lymphohistiocytosis, Hemophagocytic; Male; Syndrome; Wolman Di | 2023 |
Benign Pancreatic Hyperenzymemia: Lights on a Clinical Challenge.
Topics: Amylases; Humans; Isoamylase; Lipase; Pancreas; Pancreatic Diseases; Practice Guidelines as Topic; S | 2017 |
Chanarin-Dorfman syndrome: deficiency in CGI-58, a lipid droplet-bound coactivator of lipase.
Topics: 1-Acylglycerol-3-Phosphate O-Acyltransferase; Adipocytes; Carrier Proteins; Enzyme Activation; Fatty | 2009 |
[Genodermatosis affecting the hair: new light on well-known entities].
Topics: Alopecia; Animals; Hair Diseases; Humans; Hypertrichosis; Lipase; Mice; Mice, Hairless; Receptors, P | 2010 |
[Pancreatic hyperenzymemia: new advances in the field of clinical-diagnostic approach, with particular attention about Gullo's syndrome].
Topics: Amylases; Gastrointestinal Diseases; Humans; Isoamylase; Kidney; Lipase; Liver; Pancreas; Pancreatic | 2012 |
Disorders of lipid absorption.
Topics: Abetalipoproteinemia; Abnormalities, Multiple; Bile Acids and Salts; Bile Ducts; Celiac Disease; Chi | 1982 |
Hereditary disease of the exocrine pancreas.
Topics: Adolescent; Adult; alpha 1-Antitrypsin Deficiency; Child; Child, Preschool; Cystic Fibrosis; Exocrin | 1982 |
Lipoproteins, lipases, and the metabolic cardiovascular syndrome.
Topics: Blood Glucose; Cardiovascular Diseases; Coronary Disease; Down-Regulation; Eating; Fatty Acids, None | 1992 |
1 trial available for 1-anilino-8-naphthalenesulfonate and Syndrome
| Article | Year |
|---|---|
Free fatty acid metabolism during fenofibrate treatment of the metabolic syndrome.
Topics: Adipose Tissue; Cholesterol; Cholesterol, HDL; Cholesterol, VLDL; Fatty Acids, Nonesterified; Fenofi | 2003 |
56 other studies available for 1-anilino-8-naphthalenesulfonate and Syndrome
| Article | Year |
|---|---|
A rare case of lipase hypersecretion syndrome.
Topics: Aged; Arthritis; Eosinophilia; Humans; Lipase; Male; Necrosis; Neoplasm Invasiveness; Neoplasm Metas | 2022 |
Clinical Case Report of Familial Benign Pancreatic Hyperenzymemia.
Topics: Adolescent; Adult; Aged; Amylases; Child; Family Health; Female; Humans; Lipase; Male; Pancreatic Di | 2018 |
Man with epigastric pain and persistently elevated serum lipase.
Topics: Abdominal Pain; Aged; Humans; Lipase; Male; Pancreas; Pancreatic Diseases; Predictive Value of Tests | 2019 |
A novel mutation, c.699C>G (p.C233W), in the LIPH gene leads to a loss of the hydrolytic activity and the LPA6 activation ability of PA-PLA1α in autosomal recessive wooly hair/hypotrichosis.
Topics: Adult; Alopecia; Amino Acid Sequence; Amino Acid Substitution; Base Sequence; DNA; Female; Genes, Re | 2013 |
Healthy Chinese with benign pancreatic hyperenzymemia.
Topics: Amylases; Humans; Lipase; Male; Middle Aged; Pancreatic Diseases; Syndrome | 2015 |
SPINK1 and PRSS1 mutations in benign pancreatic hyperenzymemia.
Topics: Adolescent; Adult; Aged; Amylases; Base Sequence; Carrier Proteins; Child; Exons; Female; Genetic Pr | 2008 |
CGI-58, the causative gene for Chanarin-Dorfman syndrome, mediates acylation of lysophosphatidic acid.
Topics: 1-Acylglycerol-3-Phosphate O-Acyltransferase; Acylation; Adipose Tissue, White; Animals; Esterases; | 2008 |
Growth retardation, impaired triacylglycerol catabolism, hepatic steatosis, and lethal skin barrier defect in mice lacking comparative gene identification-58 (CGI-58).
Topics: 1-Acylglycerol-3-Phosphate O-Acyltransferase; Animals; Animals, Newborn; Animals, Suckling; Carboxyl | 2010 |
Transarterial chemoembolization of liver metastases as symptomatic therapy of lipase hypersecretion syndrome.
Topics: Aged; Carcinoma, Acinar Cell; Chemoembolization, Therapeutic; Humans; Lipase; Liver Neoplasms; Male; | 2012 |
Low serum pancreatic enzyme levels predict mortality and are associated with malnutrition-inflammation-atherosclerosis syndrome in patients with chronic kidney disease.
Topics: alpha-Amylases; Atherosclerosis; Cross-Sectional Studies; Female; Humans; Inflammation; Lipase; Male | 2013 |
[Discrepancies in the measurement of serum pancreatic lipase activities by non-enzymatic and enzymatic assays, and relationships to pseudohyperlipasemia].
Topics: Acute Disease; Biomarkers; Clinical Enzyme Tests; Colorimetry; Coronary Disease; False Positive Reac | 2002 |
Effect of secretin on serum pancreatic enzymes and on the Wirsung duct in chronic nonpathological pancreatic hyperenzymemia.
Topics: Adult; Aged; Case-Control Studies; Chronic Disease; Female; Humans; Injections, Intravenous; Isoamyl | 2003 |
[Research on the clearing factor during psychiatric syndromes].
Topics: Humans; Lipase; Mental Disorders; Research; Syndrome | 1957 |
[Syndrome of metastasizing lipaseforming pancreatic adenoma. With a contribution to the differential diagnosis of Pfeifer-Weber-Christian disease].
Topics: Adenoma; Diagnosis, Differential; Humans; Lipase; Pancreatic Neoplasms; Panniculitis; Panniculitis, | 1963 |
[COMBINED SUBSTITUTION THERAPY OF DYSPEPTIC SYNDROMES].
Topics: Chymotrypsin; Dehydrocholic Acid; Dyspepsia; Humans; Lipase; Papain; Pepsin A; Piperazines; Syndrome | 1964 |
Truncation of CGI-58 protein causes malformation of lamellar granules resulting in ichthyosis in Dorfman-Chanarin syndrome.
Topics: 1-Acylglycerol-3-Phosphate O-Acyltransferase; Adolescent; Epidermis; Esterases; Fluorescent Antibody | 2003 |
Steatohepatitis and unsuspected micronodular cirrhosis in Dorfman-Chanarin syndrome with documented ABHD5 mutation.
Topics: 1-Acylglycerol-3-Phosphate O-Acyltransferase; Child; Esterases; Fatty Liver; Female; Hepatitis; Huma | 2004 |
CGI-58 interacts with perilipin and is localized to lipid droplets. Possible involvement of CGI-58 mislocalization in Chanarin-Dorfman syndrome.
Topics: 1-Acylglycerol-3-Phosphate O-Acyltransferase; 3T3-L1 Cells; Adipocytes; Amino Acid Sequence; Animals | 2004 |
Studies on toxic oil syndrome: stereoselective hydrolysis of 3-(phenylamino)propane-1,2-diol esters by human pancreatic lipase.
Topics: Brassica rapa; Fatty Acids, Monounsaturated; Humans; Hydrolysis; Lipase; Pancreas; Plant Oils; Poiso | 2004 |
CGI-58/ABHD5 gene is mutated in Dorfman-Chanarin syndrome.
Topics: 1-Acylglycerol-3-Phosphate O-Acyltransferase; Abnormalities, Multiple; Esterases; Genes, Recessive; | 2004 |
Valproic acid-induced pancreatitis in childhood epilepsy: case series and review.
Topics: Adolescent; Anticonvulsants; Child; Child, Preschool; Diagnosis, Differential; Dose-Response Relatio | 2004 |
Two new mutations of the ABHD5 gene in a new adult case of Chanarin Dorfman syndrome: an uncommon lipid storage disease.
Topics: 1-Acylglycerol-3-Phosphate O-Acyltransferase; Adult; Age Factors; Biopsy, Needle; Esterases; Follow- | 2005 |
Erythrokeratoderma variabilis-like ichthyosis in Chanarin-Dorfman syndrome.
Topics: 1-Acylglycerol-3-Phosphate O-Acyltransferase; Child, Preschool; Esterases; Humans; Ichthyosiform Ery | 2005 |
Benign pancreatic hyperenzymemia or Gullo's syndrome.
Topics: Amylases; Humans; Lipase; Pancreatic Diseases; Pancreatic Neoplasms; Reproducibility of Results; Syn | 2006 |
Severe oily ichthyosis in monozygotic twins mimicking Chanarin-Dorfman syndrome but not associated with a mutation of the CGI58 gene.
Topics: 1-Acylglycerol-3-Phosphate O-Acyltransferase; Adult; Diagnosis, Differential; Diseases in Twins; Est | 2006 |
Fat breakdown: a function for CGI-58 (ABHD5) provides a new piece of the puzzle.
Topics: 1-Acylglycerol-3-Phosphate O-Acyltransferase; Adipose Tissue; Animals; Enzyme Activation; Esterases; | 2006 |
Adipose triglyceride lipase-mediated lipolysis of cellular fat stores is activated by CGI-58 and defective in Chanarin-Dorfman Syndrome.
Topics: 1-Acylglycerol-3-Phosphate O-Acyltransferase; 3T3-L1 Cells; Adipose Tissue; Animals; Carboxylic Este | 2006 |
Barrier dysfunction and pathogenesis of neutral lipid storage disease with ichthyosis (Chanarin-Dorfman syndrome).
Topics: 1-Acylglycerol-3-Phosphate O-Acyltransferase; Adult; Child; Epidermis; Esterases; Family Health; Fem | 2006 |
A novel S115G mutation of CGI-58 in a Turkish patient with Dorfman-Chanarin syndrome.
Topics: 1-Acylglycerol-3-Phosphate O-Acyltransferase; Epidermis; Esterases; Female; Granulocytes; Heterozygo | 2007 |
Novel duplication mutation in the patatin domain of adipose triglyceride lipase (PNPLA2) in neutral lipid storage disease with severe myopathy.
Topics: Adult; Biopsy; DNA Mutational Analysis; Female; Genetic Markers; Genetic Predisposition to Disease; | 2007 |
Clinical and genetic characterization of Chanarin-Dorfman syndrome.
Topics: 1-Acylglycerol-3-Phosphate O-Acyltransferase; Adolescent; Adult; Child; Child, Preschool; DNA Mutati | 2008 |
Chanarin-Dorfman syndrome caused by a novel splice site mutation in ABHD5.
Topics: 1-Acylglycerol-3-Phosphate O-Acyltransferase; Child; Consanguinity; Diagnosis, Differential; Hepatom | 2008 |
Pancreatic supplementation in end-stage renal disease.
Topics: Humans; Kidney Failure, Chronic; Lipase; Male; Middle Aged; Pancreatic Diseases; Pancreatic Extracts | 1984 |
Steatorrhea and pancreatic insufficiency in Shwachman syndrome.
Topics: Adolescent; Aging; Agranulocytosis; Celiac Disease; Child; Child, Preschool; Cystic Fibrosis; Dietar | 1982 |
Toxin and enzyme characterization of Staphylococcus aureus isolates from patients with and without toxic shock syndrome.
Topics: Bacterial Toxins; Child; Female; Hemolysin Proteins; Humans; Lipase; Menstruation; Micrococcal Nucle | 1982 |
Neutral lipid storage with acid lipase deficiency: a new variant of Wolman's disease with features of the Senior syndrome.
Topics: Child; Cholesterol Esters; Female; Humans; Kidney; Lipase; Lipid Metabolism; Lipid Metabolism, Inbor | 1982 |
Pulmonary embolic syndrome caused by cementing of hip endoprosthesis.
Topics: Bone Cements; Hip Prosthesis; Humans; Lipase; Oxygen; Pulmonary Embolism; Syndrome; Triglycerides | 1980 |
Prenatal monitoring for Wolman's disease in a pregnancy at risk: first case in the Federal Republic of Germany.
Topics: Adrenal Gland Diseases; Amniotic Fluid; Female; Humans; Lipase; Pregnancy; Prenatal Diagnosis; Syndr | 1981 |
Gut inflammation in children with cystic fibrosis on high-dose enzyme supplements.
Topics: Adolescent; Albumins; alpha 1-Antitrypsin; Amylases; Bromelains; Case-Control Studies; Child; Child, | 1995 |
Changes of lipolytic enzymes cluster with insulin resistance syndrome. Botnia Study Group.
Topics: Analysis of Variance; Blood Glucose; Blood Pressure; Cholesterol; Cohort Studies; Diabetes Mellitus, | 1995 |
Pathophysiology of the pancreatic defect in Johanson-Blizzard syndrome: a disorder of acinar development.
Topics: Case-Control Studies; Colipases; Consanguinity; Cystic Fibrosis; Exocrine Pancreatic Insufficiency; | 1994 |
Gut inflammation in children with cystic fibrosis on high-dose enzyme supplementation.
Topics: Amylases; Bromelains; Child; Child, Preschool; Cystic Fibrosis; Drug Combinations; Humans; Inflammat | 1996 |
Increased spontaneous chromosomal breakage in Shwachman syndrome.
Topics: Amylases; Bone Diseases, Developmental; Celiac Disease; Chromosome Breakage; Diarrhea; Exocrine Panc | 1999 |
Effects of inhibitors of the activity of poly (ADP-ribose) synthetase on the organ injury and dysfunction caused by haemorrhagic shock.
Topics: Alanine Transaminase; Animals; Aspartate Aminotransferases; Benzamides; Blood Pressure; Creatine Kin | 1999 |
Calpain inhibitor I reduces the activation of nuclear factor-kappaB and organ injury/dysfunction in hemorrhagic shock.
Topics: Animals; Blood Pressure; Cyclooxygenase 2; DNA; Glycoproteins; Heart Rate; I-kappa B Proteins; Intes | 2001 |
Mutations in CGI-58, the gene encoding a new protein of the esterase/lipase/thioesterase subfamily, in Chanarin-Dorfman syndrome.
Topics: 1-Acylglycerol-3-Phosphate O-Acyltransferase; Adolescent; Adult; Amino Acid Motifs; Base Sequence; C | 2001 |
Genetic variation of lysosomal acid lipase.
Topics: Cholesterol Esters; Electrophoresis; Female; Fibroblasts; Humans; Infant; Leukocytes; Lipase; Lipid | 1976 |
Acid lipase: a histochemical and biochemical study using triton X100-naphtyl palmitate micelles.
Topics: Animals; Colloids; Culture Techniques; Esterases; Haplorhini; Histocytochemistry; History, 18th Cent | 1978 |
[Wolman's disease].
Topics: Cholesterol Esters; Humans; Lipase; Lipidoses; Syndrome; Triglycerides; Xanthomatosis | 1978 |
Fat embolism syndrome: a puzzling phenomenon.
Topics: Embolism, Fat; Fractures, Bone; Heparin; Humans; Lipase; Syndrome | 1977 |
Partial deficiency of acid lipase with storage of triglycerides and cholesterol esters in liver. Genetic variant of Wolman's disease?
Topics: Child; Cholesterol; Cholesterol Esters; Chromatography, Thin Layer; Fatty Liver; Humans; Lipase; Lip | 1976 |
[The formation of a hypokinetic syndrome of the digestive system under conditions of weightlessness].
Topics: Amylases; Digestive System; Digestive System Diseases; Humans; Lipase; Pepsinogens; Space Flight; Sy | 1992 |
Exocrine pancreatic insufficiency-like syndrome in giraffe.
Topics: Amylases; Animals; Artiodactyla; Diarrhea; Exocrine Pancreatic Insufficiency; Feces; Lipase; Pancrea | 1991 |
Use of Nile red stain in the detection of cholesteryl ester accumulation in acid lipase-deficient fibroblasts.
Topics: Cholesterol Esters; Chromatography, Thin Layer; Fibroblasts; Fluorescent Dyes; Humans; Lipase; Metab | 1988 |
Lipid accumulation and acid lipase deficiency in fibroblasts from a family with Wolman's disease, and their apparent correction in vitro.
Topics: Adult; Cells, Cultured; Child; Cholesterol; Female; Fibroblasts; Humans; Lipase; Lipidoses; Male; Me | 1972 |
Reinvestigation of the pathogenesis of familial xanthomatosis through conjoint cytochemical, ultrastructural, and biochemical studies.
Topics: Adrenal Glands; Diseases in Twins; Humans; Infant; Intestine, Small; Lipase; Lipid Metabolism; Lipid | 1972 |