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| | Birth Disorder Information Directory - G |
 | | Gilbert('s) Syndrome (Gilbert Lereboullet Syndrome, Hyperbilirubinemia I, Icterus Intermittens Juvenalis, Meulengracht's Disease, Unconjugated Benign Bilirubinemia) | | | Gorlin Chaudry Moss Syndrome (Craniofacial Dysostosis Genital Dental Cardiac Anomalies) | | | Gitelman's syndrome is genetically distinct from other forms of Bartter's syndrome |
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http://www.bdid.com/defectg.htm
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| | Birth Disorder Information Directory - G |
| | Gilbert('s) Syndrome (Gilbert Lereboullet Syndrome, Hyperbilirubinemia I, Icterus Intermittens Juvenalis, Meulengracht's Disease, Unconjugated Benign Bilirubinemia) | | | Gorlin Chaudry Moss Syndrome (Craniofacial Dysostosis Genital Dental Cardiac Anomalies) | | | Gitelman's syndrome is genetically distinct from other forms of Bartter's syndrome |
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http://www.bdid.com/defectg.htm
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| | List of diseases starting with G: Encyclopedia topic |
| | Gilbert's syndrome (Gilbert's syndrome: gilberts syndrome or familial benign unconjugated hyperbilirubinaemia is a genetic... | | | Gardner's syndrome (Gardner's syndrome: gardners syndrome is a condition affecting the digestive tract.... | | | Guillain-Barré syndrome (Guillain-Barré syndrome: A form of peripheral polyneuritis characterized by pain and weakness and sometimes paralysis of the limbs; cause is unknown) |
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http://www.absoluteastronomy.com/reference/list_of_diseases_starting_with_g
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| | eMedicine - Fitz-Hugh-Curtis Syndrome : Article by Michael M Frumovitz, MD |
| | Gilbert DN, Moellering RC Jr, Sande MA: The Sanford Guide to Antimicrobial Therapy. | | | Most cases are asymptomatic (ie, difficult to diagnose clinically) and are diagnosed only at the time of surgery, when FHC syndrome is in the chronic stage. | | | Background: Originally described in 1920, Fitz-Hugh-Curtis (FHC) syndrome (formally known as Fitz-Hugh and Curtis syndrome) consists of right upper quadrant pain resulting from ascending pelvic infection and inflammation of the liver capsule or diaphragm. |
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http://www.emedicine.com/med/topic797.htm
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| | genetable2.html |
| | DRN1; Deoxyribonuclease I Precursor (DNase I) Gilbert's Syndrome | | | Alport Syndrome (similar to canine x-linked hereditary nephritis (HN)) | | | ALK1; MPI; Antileukoproteinase 1; ALP; HUSI-1; Seminal proteinase inhibitor; secretory leukocyte protease inhibitor; BLPI; Mucos proteinase inhibitor |
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http://www-nmr.cabm.rutgers.edu/labdocuments/bioinforminfo/genetable2.html
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| | genetable2.html |
| | DRN1; Deoxyribonuclease I Precursor (DNase I) Gilbert's Syndrome | | | Alport Syndrome (similar to canine x-linked hereditary nephritis (HN)) | | | DCRA; Down syndrome critical region protein A; in PEP8/H58 family. |
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http://www-nmr.cabm.rutgers.edu/labdocuments/bioinforminfo/genetable2.html
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| | GENERAL SURGERY LINKS |
| | Acute Mesenteric Ischemia Chronic Mesenteric Ischemia Constipation Malignant Carcinoid Syndrome Crigler-Najjar Syndrome Familial Adenomatous Polyposis Gilbert Syndrome Irritable Bowel Syndrome Peutz-Jeghers Syndrome Ulcerative Colitis | | | Boerhaave Syndrome Esophageal Varices Gastroesophageal Reflux Disease Hiatal Hernia Mallory-Weiss Tear | | | Hepatic Cystadenomas Hepatic Carcinoma, Primary Hepatic Failure Hepatocellular Adenoma Hepatorenal Syndrome |
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http://www.geocities.com/alghamdi83/gs.html
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| | Androgen Insensitivity Syndrome |
| | [Androgen Resistance Syndrome, Testicular Feminization Syndrome, Feminizing Testes Syndrome, Male Pseudo-hermaphroditism, Morris's Syndrome (CAIS), Goldberg-Maxwell Syndrome, Reifenstein Syndrome (PAIS), Gilbert-Dreyfus Syndrome, Lubs Syndrome] |
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http://www.kumc.edu/gec/support/androgen.html
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| | testicular feminization syndrome : Definition |
| | Also known as Androgen Insensitivity Syndrome, Androgen Resistance Syndrome, Feminizing Testes Syndrome (Feminising Testes Syndrome), Male Pseudo-hermaphroditism, Morris's Syndrome (CAIS), Goldberg-Maxwell Syndrome, Reifenstein Syndrome (PAIS), Gilbert-Dreyfus Syndrome (PAIS), Rosewater Syndrome (PAIS), Lubs Syndrome (PAIS). | | | Search for testicular feminization syndrome in these other databases too | | | A human condition, inherited as an X-linked recessive, caused by a mutation in a gene coding for the androgen (testosterone) receptor, in which genetical (XY) males develop female secondary sexual characters. |
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http://www.biology-text.com/definition.php?word=testicular+feminization+syndrome
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| | gilbert brown - Definition and Meaning of gilbert brown |
| | 5:...rt syndrome, the chance of their transmitting the Gilbert gene to each of their children is one-half (50%)... | | | People with Gilbert syndrome are otherwise entirely normal with no ot... | | | 1:...Sullivan(noun)
1: the music of Gilbert and Sullivan; "he could sing all of |
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http://www.wordiq.com/reference/gilbert+brown
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| | Morbus Gilbert-Meulengracht |
| | Macklon AF, Savage RL, and Rawlins MD. Gilbert's syndrome and drug metabolism. | | | Gilbert's syndrome is caused by a heterozygous missense mutation in the gene for bilirubin UDP-glucuronosyltransferase. | | | Effect of bilirubin UDP glucuronosyltransferase 1 gene TATA box genotypes on serum bilirubin concentrations in chronic liver injuries. |
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http://www.cx.unibe.ch/ikp/lab2/Gilberte.html
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| | Genetic Interactions in the Pathogenesis of Neonatal Hyperbilirubinemia: Gilbert's Syndrome and Glucose-6-Phosphate Dehydrogenase Deficiency |
| | Whereas G-6-PD deficiency or Gilbert's Syndrome, alone, did not predispose to hyperbilirubinemia, G-6-PD deficient neonates who also were heterozygotes or homozygotes for the variant UGT gene promoter did have significantly increased incidences of hyperbilirubinemia. | | | This review highlights the major clinical features of both Gilbert's Syndrome and G-6-PD deficiency, and surveys a series of studies related to neonatal jaundice in G-6-PD deficient neonates culminating in the documentation of an interaction between the two conditions that is crucial to the pathogenesis of hyperbilirubinemia. | | | Glucose-6-phosphate dehydrogenase (G-6-PD) deficiency is a common condition with a worldwide distribution that has the potential for causing severe hyperbilirubinemia with bilirubin encephalopathy. |
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http://www.nature.com/cgi-taf/DynaPage.taf?file=/jp/journal/v21/n1s/abs/7210630a.html
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| | Hockey Trade Rumors - Hockey Information and Rumors - TSN.ca reporting two Buffalo players ill with potential SARS |
| | Gilbert stressed the decision to hold the players back was a precaution, and that neither has shown any signs of being infected with Severe Acute Respiratory Syndrome. | | | It was determined that there was what Gilbert called ``a remote chance'' that the players had limited exposure to the virus after Campbell's relative visited them earlier in the week. | | | Sabres spokesman Mike Gilbert announced that Rhett Warrener and Brian Campbell, who played in Friday night's 4-1 win over Montreal, did not travel with the team for its game at Carolina on Saturday. |
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http://www.hockeytraderumors.com/modules.php?name=News&file=print&sid=2799
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| | Bilirubin metabolism - encyclopedia article about Bilirubin metabolism. |
| | ICD-9 code: 277.4 Gilbert's syndrome, often shortened to the acronym GS, is a genetic disorder of bilirubin metabolism, found in about 5% of the population. | | | ICD-9 code: 277.4 Crigler-Najjar syndrome is a disorder of bilirubin metabolism. | | | It can be treated in youth with special lights designed to aid in the breakdown of bilirubin. |
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http://encyclopedia.thefreedictionary.com/Bilirubin+metabolism
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| | eMedicine - Crigler-Najjar Syndrome : Article Excerpt by: Alessio Pigazzi, MD, PhD |
| | Synonyms, Key Words, and Related Terms: CNS, Crigler-Najjar disease, Gilbert syndrome, Arias syndrome, congenital nonhemolytic jaundice, neonatal jaundice, inherited unconjugated hyperbilirubinemias, uridine diphosphate glycosyltransferase, UGT, kernicterus, bilirubin encephalopathy, plasma exchange transfusion | | | CNS is elicited by a lack or deficiency of the enzyme uridine diphosphate glycosyltransferase (UGT). | | | Type 1 CNS is associated with an almost complete absence of the enzyme, which results in very high levels of unconjugated hyperbilirubinemia (up to 50 mg/dL) at birth. |
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http://www.emedicine.com/med/byname/crigler-najjar-syndrome.htm
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| | 1 |
| | Oner R, Acar C, Oner C, Yenicesu I, Gumruk F, Gurgey A, Altay C. Chronic hemolytic anemia associated with glucose 6-phosphate dehydrogenase (Guadalajara)1 159 C --> T (387 Arg --> Cys) deficiency associated with Gilbert syndrome in a Turkish patient. | | | Koc A, Oner R, Oner C, Aktas D, Sozen M, Tuncbilek E, Altay C. Myelodysplastic syndrome (MDS) associated with increased hemoglobin F and trisomy 8: presentation of a patient. | | | Dominant beta-thalassaemia trait in a Portuguese family is caused by a deletion of (G)TGGCTGGTGT(G) and an insertion of (G)GCAG(G) in codons 134, 135, 136 and 137 of the beta-globin gene. |
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http://yunus.hacettepe.edu.tr/~roner/yayin.htm
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| | JAUNDICE |
| | Conditions that can result in jaundice include: drug side effects, drug-induced hepatitis, pancreatic cancer, cholangiocarcinoma, choledocholithiasis, biliary atresia, bile duct stricture, Gilbert's syndrome, Dubin-Johnson syndrome, cholestasis of pregnancy, newborn jaundice, blood transfusion reaction, hemolytic anemia, viral hepatitis, primary biliary cirrhosis, autoimmune hepatitis, chronic active hepatitis, and malaria. | | | A yellowing of the skin, eyes, and sublingual (under the tongue) area that occurs when there is an overabundance of bilirubin in the bloodstream. |
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http://www.medhelp.org/glossary2/new/GLS_2786.HTM
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| | Dyschondrosteoses |
| | Petrella R, Ludman MD, Rabinowitz JG, Gilbert F, Hirschhorn K. Mesoamerica dysplasia with absence of fibulae and hexadactyly: Nievergelt syndrome or new syndrome? |
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http://www.stevensorenson.com/residents6/dyschondrosteoses.htm
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| | Gilbert Breschet (www.whonamedit.com) |
| | A very rare syndrome marked by the gradual and often complete circumscribed spontaneous resorption of bone tissue or a group of bones. | | | Following his medical studies at the University of Paris, Gilbert Breschet was conferred doctor of medicine at the University of Paris in 1812, with a dissertation based on some of the thoughts of François Joseph Victor Broussais (1772-1838), but worked over in a highly original way by Breschet. | | | After receiving his doctorate he settled in Paris. |
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http://www.whonamedit.com/doctor.cfm/2698.html
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| | Medical Testing Articles Notes |
| | Liver Problems: Gilbert's Syndrome - a relatively common and benign congenital (probably hereditary) liver disorder, found more frequently in males. | | | Since you can have kidney disease without any symptoms, your doctor may first detect the condition through routine blood and urine tests. | | | Liver Problems: Hemochromatosis - a genetic condition that causes the body to absorb and store too much iron. |
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http://aaaaq.com/medical_testing/articles.html
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| | Clinical Study: 04-C-0031, Phase I Trial of Medi-507 in CD2-Positive Lymphoproliferative Disease |
| | Serum glutamic oxaloacetic transaminase (SGOT) and serum glutamate pyruvate transaminase (SGPT) value less than or equal to 2.0-fold greater than the upper limit of normal and bilirubin less than or equal to 2.0 mg/dL unless due to Gilbert's syndrome (unconjugated hyperbilirubinemia) in which case the bilirubin should be less than or equal to 3.5 mg/dL. | | | Prior treatment with cytotoxic chemotherapy, surgery, and prolonged cytolytic steroid therapy is allowed provided last treatment was given at least 3 weeks prior to first dose of study drug administration and all toxicities have resolved. | | | For patients with LGL leukemia, ANC and platelet count will not be considered in determining study eligibility. |
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http://clinicalstudies.info.nih.gov/detail/A_2004-C-0031.html
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| | Nat'l Academies Press, The Medical Follow-up Agency: (1999), 4 Recent Decades |
| | Such a data base would be useful in controlling for the so-called healthy veteran syndrome, which postulated that men on the MFUA's veteran rosters were less susceptible to disease than the general population since they had passed the physical exami- nation on induction. | | | Lack of core funding was a key dilemma, and Gilbert Beebe acted from his "advisory" role to provide it. | | | In fact, no studies of trauma were being undertaken, in part because methods of treating trauma in the 1970s were so different from those used in World War II. |
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http://books.nap.edu/books/0309064406/html/53.html
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| | Rotavirus |
| | Influenza viruses A, B and C are ubiquitous and cause common respiratory illnesses in persons of all ages referred to as "common cold syndrome". | | | The short duration of ribavirin aerosol for the treatment of influenza virus in mice and HRSV infections in cotton rats was studied (Gilbert et al., 1992). | | | The virus causes diarrheal disease, especially in children and until today, there is no specific treatment. |
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http://www.ophidia.com/Rotaviru.htm
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| | Shai Hulud |
| | Josh: Shai Hulud syndrome is when a band says were going to take three years to write an album whether you like it or not. | | | I still want people to look at Shai Hulud as the best that it ever was or better, and its not hard to fill the shoes of Chad Gilbert because I think he has an awesome voice. | | | Shai Hulud has been my favorite hardcore band since the first EP came out, so for the first year I couldnt believe it and it was like a dream come true. |
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http://www.angelfire.com/geek/nca/shaihulud.html
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| | Carol Enns Professional Publications |
| | Enns, C.Z. The politics and psychology of "false memory syndrome." In J.C. Chrisler, C. | | | Enns, C. A., Campbell, J., Courtois, C., Gottlieb, M., Lese, K., Gilbert, M., and Forrest, L., (1998). | | | Phelps, A., Friedlander, M., and Enns, C. Psychotherapy process variables associated with the retrieval of memories of childhood abuse: A qualitative study. |
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http://people.cornellcollege.edu/cenns/pub1.html
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| | DADES DEL SUMARI DE BLOOD CELLS MOLECULES AND DISEASES |
| | Títol: Severe Jaundice in a Patient with a Previously Undescribed Glucose-6-phosphate Dehydrogenase (G6PD) Mutation and Gilbert Syndrome. | | | Títol: Control of Analyzer Slope and Intercept in the Measurement of Packed Red Cell Volume (PCV): Part I. Autor: Bull, Brian S.; Cacho, Vince P. R.; Hay, Karen L. pg - 108 |
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http://sumaris.cbuc.es/cgis/sumari.cgi?issn=10799796&idsumari=A2002N000002V000028
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| | CO-CURE Archives -- February 2000, week 2 (#9) |
| | Dr Gilbert and colleagues seek to discredit the authors of the book under review[2] for having come to their conclusions before the Centers for Disease Control and Prevention classification was published. | | | Chronic fatigue syndrome follows the now-discarded diagnoses of railway spine,[1] neurasthenia, and countless other alleged diseases favored by trial lawyers. |
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http://listserv.nodak.edu/cgi-bin/wa.exe?A2=ind0002b&L=co-cure&F=&S=&P=1330
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