|
| |
| | Birth Disorder Information Directory - G |
 | | <<b>bb>>Gilbert<b>bb>>('<b>sb>) Syndrome (<<b>bb>>Gilbert<b>bb>> Lereboullet Syndrome, Hyperbilirubinemia I, Icterus Intermittens Juvenalis, Meulengracht'<b>sb> Disease, Unconjugated Benign Bilirubinemia) |  | | Gitelman'<b>sb> syndrome is genetically distinct from other forms of Bartter'<b>sb> syndrome |  | | Gershinibaruch Leibo Syndrome (Aplasia Cutis with High Myopia and Cone-Rod Dysfunction) |
|
http://www.bdid.com/defectg.htm
(302 words)
|
|
| |
| | Birth Disorder Information Directory - G |
 | | <<b>bb>>Gilbert<b>bb>>('<b>sb>) Syndrome (<<b>bb>>Gilbert<b>bb>> Lereboullet Syndrome, Hyperbilirubinemia I, Icterus Intermittens Juvenalis, Meulengracht'<b>sb> Disease, Unconjugated Benign Bilirubinemia) |  | | Gitelman'<b>sb> syndrome is genetically distinct from other forms of Bartter'<b>sb> syndrome |  | | Gorlin Chaudry Moss Syndrome (Craniofacial Dysostosis Genital Dental Cardiac Anomalies) |
|
http://www.bdid.com/defectg.htm
(302 words)
|
|
| |
| | List of diseases starting with G: Encyclopedia topic |
 | | <<b>bb>>Gilbert<b>bb>>'<b>sb> syndrome (<<b>bb>>Gilbert<b>bb>>'<b>sb> syndrome: gilberts syndrome or familial benign unconjugated hyperbilirubinaemia is a genetic... |  | | 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) |  | | Granulocytopenia (Granulocytopenia: An acute blood disorder (often caused by radiation or drug therapy) characterized by severe reduction in granulocytes) |
|
http://www.absoluteastronomy.com/reference/list_of_diseases_starting_with_g
(530 words)
|
|
| |
| | eMedicine - Fitz-Hugh-Curtis Syndrome : Article by Michael M Frumovitz, MD |
 | | <<b>bb>>Gilbert<b>bb>> DN, Moellering RC Jr, Sande MA: The Sanford Guide to Antimicrobial Therapy. |  | | 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. |  | | Treat the patient'<b>sb> sexual partner for gonorrhea and chlamydia. |
|
http://www.emedicine.com/med/topic797.htm
(530 words)
|
|
| |
| | genetable2.html |
 | | DRN1; Deoxyribonuclease I Precursor (DNase I) <<b>bb>>Gilbert<b>bb>>'<b>sb> Syndrome |  | | ALK1; MPI; Antileukoproteinase 1; ALP; HUSI-1; Seminal proteinase inhibitor; secretory leukocyte protease inhibitor; BLPI; Mucos proteinase inhibitor |  | | UDP-Glucuronosyltransferase 1-1; UGT-1A; UGT1-01; Bilirubin Specific isozyme 1; HUG-BR1; |
|
http://www-nmr.cabm.rutgers.edu/labdocuments/bioinforminfo/genetable2.html
(1769 words)
|
|
| |
| | genetable2.html |
 | | DRN1; Deoxyribonuclease I Precursor (DNase I) <<b>bb>>Gilbert<b>bb>>'<b>sb> Syndrome |  | | Alport Syndrome (similar to canine x-linked hereditary nephritis (HN)) |  | | DCRA; Down syndrome critical region protein A; in PEP8/H58 family. |
|
http://www-nmr.cabm.rutgers.edu/labdocuments/bioinforminfo/genetable2.html
(1769 words)
|
|
| |
| | GENERAL SURGERY LINKS |
 | | Acute Mesenteric Ischemia Chronic Mesenteric Ischemia Constipation Malignant Carcinoid Syndrome Crigler-Najjar Syndrome Familial Adenomatous Polyposis <<b>bb>>Gilbert<b>bb>> Syndrome Irritable Bowel Syndrome Peutz-Jeghers Syndrome Ulcerative Colitis |  | | Boerhaave Syndrome Esophageal Varices Gastroesophageal Reflux Disease Hiatal Hernia Mallory-Weiss Tear |  | | Goiter Goiter, Diffuse Toxic Wermer Syndrome (MEN Type 1) Multiple Endocrine Neoplasia, Type II Thyroid Nodule Thyroiditis, Subacute VIPomas Acromegaly Addison Disease Adrenal Adenoma Thymoma Hurthle Cell Carcinoma Thyroid Lymphoma Thyroid, Anaplastic Carcinoma Thyroid, Medullary Carcinoma |
|
http://www.geocities.com/alghamdi83/gs.html
(1769 words)
|
|
| |
| | Androgen Insensitivity Syndrome |
 | | [Androgen Resistance Syndrome, Testicular Feminization Syndrome, Feminizing Testes Syndrome, Male Pseudo-hermaphroditism, Morris'<b>sb> Syndrome (CAIS), Goldberg-Maxwell Syndrome, Reifenstein Syndrome (PAIS), <<b>bb>>Gilbert<b>bb>>-Dreyfus Syndrome, Lubs Syndrome] |
|
http://www.kumc.edu/gec/support/androgen.html
(65 words)
|
|
| |
| | testicular feminization syndrome : Definition |
 | | Also known as Androgen Insensitivity Syndrome, Androgen Resistance Syndrome, Feminizing Testes Syndrome (Feminising Testes Syndrome), Male Pseudo-hermaphroditism, Morris'<b>sb> Syndrome (CAIS), Goldberg-Maxwell Syndrome, Reifenstein Syndrome (PAIS), <<b>bb>>Gilbert<b>bb>>-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. |
|
http://www.biology-text.com/definition.php?word=testicular+feminization+syndrome
(86 words)
|
|
| |
| | <<b>bb>>gilbert<b>bb>> brown - Definition and Meaning of <<b>bb>>gilbert<b>bb>> brown |
 | | 5:...rt syndrome, the chance of their transmitting the <<b>bb>>Gilbert<b>bb>> gene to each of their children is one-half (50%)... |  | | People with <<b>bb>>Gilbert<b>bb>> syndrome are otherwise entirely normal with no ot... |  | | 1:...Sullivan(noun) 1: the music of <<b>bb>>Gilbert<b>bb>> and Sullivan; "he could sing all of |
|
http://www.wordiq.com/reference/gilbert+brown
(86 words)
|
|
| |
| | Morbus <<b>bb>>Gilbert<b>bb>>-Meulengracht |
 | | Macklon AF, Savage RL, and Rawlins MD. <<b>bb>>Gilbert<b>bb>>'<b>sb> syndrome and drug metabolism. |  | | <<b>bb>>Gilbert<b>bb>>'<b>sb> 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. |
|
http://www.cx.unibe.ch/ikp/lab2/Gilberte.html
(86 words)
|
|
| |
| | Hockey Trade Rumors - Hockey Information and Rumors - TSN.ca reporting two Buffalo players ill with potential SARS |
 | | <<b>bb>>Gilbert<b>bb>> 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 <<b>bb>>Gilbert<b>bb>> called ``a remote chance'' that the players had limited exposure to the virus after Campbell'<b>sb> relative visited them earlier in the week. |  | | Sabres spokesman Mike <<b>bb>>Gilbert<b>bb>> announced that Rhett Warrener and Brian Campbell, who played in Friday night'<b>sb> 4-1 win over Montreal, did not travel with the team for its game at Carolina on Saturday. |
|
http://www.hockeytraderumors.com/modules.php?name=News&file=print&sid=2799
(409 words)
|
|
| |
| | Bilirubin metabolism - encyclopedia article about Bilirubin metabolism. |
 | | ICD-9 code: 277.4 <<b>bb>>Gilbert<b>bb>>'<b>sb> 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. |
|
http://encyclopedia.thefreedictionary.com/Bilirubin+metabolism
(754 words)
|
|
| |
| | eMedicine - Crigler-Najjar Syndrome : Article Excerpt by: Alessio Pigazzi, MD, PhD |
 | | Synonyms, Key Words, and Related Terms: CNS, Crigler-Najjar disease, <<b>bb>>Gilbert<b>bb>> 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. |
|
http://www.emedicine.com/med/byname/crigler-najjar-syndrome.htm
(754 words)
|
|
| |
| | 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 <<b>bb>>Gilbert<b>bb>> 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. |
|
http://yunus.hacettepe.edu.tr/~roner/yayin.htm
(754 words)
|
|
| |
| | JAUNDICE |
 | | Conditions that can result in jaundice include: drug side effects, drug-induced hepatitis, pancreatic cancer, cholangiocarcinoma, choledocholithiasis, biliary atresia, bile duct stricture, <<b>bb>>Gilbert<b>bb>>'<b>sb> 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. |
|
http://www.medhelp.org/glossary2/new/GLS_2786.HTM
(105 words)
|
|
| |
| | Dyschondrosteoses |
 | | Petrella R, Ludman MD, Rabinowitz JG, <<b>bb>>Gilbert<b>bb>> F, Hirschhorn K. Mesoamerica dysplasia with absence of fibulae and hexadactyly: Nievergelt syndrome or new syndrome? |
|
http://www.stevensorenson.com/residents6/dyschondrosteoses.htm
(105 words)
|
|
| |
| | <<b>bb>>Gilbert<b>bb>> 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, <<b>bb>>Gilbert<b>bb>> 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. |
|
http://www.whonamedit.com/doctor.cfm/2698.html
(105 words)
|
|
| |
| | Medical Testing Articles Notes |
 | | Liver Problems: <<b>bb>>Gilbert<b>bb>>'<b>sb> 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. |
|
http://aaaaq.com/medical_testing/articles.html
(105 words)
|
|
| |
| | 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 <<b>bb>>Gilbert<b>bb>>'<b>sb> syndrome (unconjugated hyperbilirubinemia) in which case the bilirubin should be less than or equal to 3.5 mg/dL. |  | | For patients with LGL leukemia, ANC and platelet count will not be considered in determining study eligibility. |  | | Women of childbearing potential must have a negative serum pregnancy test within 5 days of the initial MEDI-507 administration and a negative urine pregnancy test on Day 0 prior to receiving the first dose of MEDI-507. |
|
http://clinicalstudies.info.nih.gov/detail/A_2004-C-0031.html
(105 words)
|
|
| |
| | 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'<b>sb> 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 <<b>bb>>Gilbert<b>bb>> 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. |
|
http://books.nap.edu/books/0309064406/html/53.html
(105 words)
|
|
| |
| | Rotavirus |
 | | Influenza viruses A, <b>Bb> 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 (<<b>bb>>Gilbert<b>bb>> et al., 1992). |  | | Committee on Infectious Diseases, (1993): Use of ribavirin in the treament of respiratory syncytial virus in infection. |
|
http://www.ophidia.com/Rotaviru.htm
(3343 words)
|
|
| |
| | 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 it<b>sb> not hard to fill the shoes of Chad <<b>bb>>Gilbert<b>bb>> 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. |
|
http://www.angelfire.com/geek/nca/shaihulud.html
(1581 words)
|
|
| |
| | Carol Enns Professional Publications |
 | | Enns, C. A., Campbell, J., Courtois, C., Gottlieb, M., Lese, K., <<b>bb>>Gilbert<b>bb>>, 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. |  | | Enns, C. On the complexities of assessing child sexual abuse disclosures. |
|
http://people.cornellcollege.edu/cenns/pub1.html
(387 words)
|
|
| |
| | 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 <<b>bb>>Gilbert<b>bb>> Syndrome. |  | | Títol: Control of Analyzer Slope and Intercept in the Measurement of Packed Red Cell Volume (PCV): Part I. Autor: Bull, Brian <b>Sb>.; Cacho, Vince P. R.; Hay, Karen L. pg - 108 |
|
http://sumaris.cbuc.es/cgis/sumari.cgi?issn=10799796&idsumari=A2002N000002V000028
(387 words)
|
|
| |
| | CO-CURE Archives -- February 2000, week 2 (#9) |
 | | Dr <<b>bb>>Gilbert<b>bb>> 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. |
|
http://listserv.nodak.edu/cgi-bin/wa.exe?A2=ind0002b&L=co-cure&F=&S=&P=1330
(387 words)
|
|
|