Zobrazeno 1 - 10
of 12
pro vyhledávání: '"G. Dean Timmons"'
Autor:
Leslie Anne Morrison, Jeffrey Buchhalter, Gregory K. Yim, Roberto Caraballo, Judy Nation, Shlomo Shinnar, David A. Griesemer, Juergen Schreck, Carmela Tardo, Eric H. Kossoff, Agustin Legido, Y.M. Christiana Liu, Russell Snyder, Roger Larson, Anne E. Anderson, J. Helen Cross, Jong M. Rho, Bruce A. Cohen, James W. Wheless, Per Åmark, Heidi H. Pfeifer, Edward Kovnar, Pierangelo Veggiotti, Leon Dure, Colette Parker, Douglas R. Nordli, Elaine C. Wirrell, Robyn Blackford, Eileen P.G. Vining, J. Ben Renfroe, G. Dean Timmons, Elizabeth A. Thiele, Brian Grabert, Mary Currey, Carl E. Stafstrom, A. G. Christina Bergqvist, Beth Zupec-Kania, Heung Dong Kim, Michael Goldstein, Joerg Klepper, Diane Donley, Bhuwan P. Garg, Maria Dahlin, Rana S. Jehle, Zahava Turner, Elizabeth J. Donner, Karen Ballaban-Gil
Publikováno v:
Epilepsia. 50:304-317
The ketogenic diet (KD) is an established, effective nonpharmacologic treatment for intractable childhood epilepsy. The KD is provided differently throughout the world, with occasionally significant variations in its administration. There exists a ne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::91f7a451482128d5d744bddff7f795e9
https://doi.org/10.1111/j.1528-1167.2008.01765.x
https://doi.org/10.1111/j.1528-1167.2008.01765.x
Publikováno v:
Clinica chimica acta; international journal of clinical chemistry. 281(1-2)
Screening tests for genetic metabolic diseases remain extremely useful due to their rapidity, ease of interpretation and substantial reduction of cost. However, interferences in these tests are still a source of concern in laboratory medicine. Cost c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b50f709c9ef3af9a57e09ead1c373005
https://pubmed.ncbi.nlm.nih.gov/10217628
https://pubmed.ncbi.nlm.nih.gov/10217628
Autor:
G. Dean Timmons
Publikováno v:
Neurology. 77:805-805
The Neurological Examination of the Child with Minor Neurological Dysfunction, 3rd edition Mijna Hadders-Algra, 132 pp., Mac Keith Press, 2010, $72 This updated version of Professors Prechtl's and Towen's 1970 edition and Professor Towen's 1979 editi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ed7504af3a1a61847104acbe91970708
https://doi.org/10.1212/wnl.0b013e31822b0181
https://doi.org/10.1212/wnl.0b013e31822b0181
Autor:
G. Dean Timmons, Martin D. Schechter
Publikováno v:
The Journal of Clinical Pharmacology. 25:276-280
Errors of commission and omission, chair movements, and reaction times were assessed in fifteen previously diagnosed hyperactive children on a Continuous Performance Test after four drug regimens: amphetamine at doses of 1.6 and 5.0 mg twice a day, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba4c0702f56bf432cac3f038c9df0427
https://doi.org/10.1002/j.1552-4604.1985.tb02838.x
https://doi.org/10.1002/j.1552-4604.1985.tb02838.x
Autor:
Robert P. Bolande, G. Dean Timmons
Publikováno v:
The Journal of Pediatrics. 79:142-150
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1adb5e2ed4b91d5dea92d5e69487e24a
https://doi.org/10.1016/s0022-3476(71)80078-1
https://doi.org/10.1016/s0022-3476(71)80078-1
Autor:
Kenneth P. Johnson, G. Dean Timmons
Publikováno v:
New England Journal of Medicine. 283:1505-1507
STENOSIS of the aqueduct of Sylvius is a common cause of human hydrocephalus, occurring most often in infancy but also in childhood and in adult life. In a small proportion of cases, aqueductal narrowing occurs in a genetically determined pattern1 or
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f665db508820b749ad3f80b276fc6ae
https://doi.org/10.1056/nejm197012312832707
https://doi.org/10.1056/nejm197012312832707
Autor:
G. Dean Timmons, Martin D. Schechter
Publikováno v:
Journal of clinical pharmacology. 25(4)
Seventy-five normal (control) children were compared to 15 hyperactive children on a Continuous Performance Test over an eight-week period. The control children were observed to have a relatively constant number of correct responses, chair movements,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21986380066f5376b8bbb04beea3352a
https://pubmed.ncbi.nlm.nih.gov/4008671
https://pubmed.ncbi.nlm.nih.gov/4008671
Publikováno v:
Clinica chimica acta; international journal of clinical chemistry. 39(2)
An improved method for the determination of arylsulfatase A, based on the ether solubility of 4-nitrocatechol, has been established. The method has been applied to the diagnosis of metachromatic leukodystrophy and can identify the carrier state. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::447cc4251595f7202ea9cecf27e1e1ed
https://pubmed.ncbi.nlm.nih.gov/5043787
https://pubmed.ncbi.nlm.nih.gov/5043787
Publikováno v:
American Journal of Diseases of Children. 127:724
A 4-year-old girl with arginosuccinic-aciduria exhibited mental retardation, seizures, ataxia, and abnormal hair. Fasting and postprandial ammonia and blood urea nitrogen levels were maintained within normal limits. The mechanism of urea synthesis, i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d62f8186d7312a01becdc84ddf25c47e
https://doi.org/10.1001/archpedi.1974.02110240110017
https://doi.org/10.1001/archpedi.1974.02110240110017
Publikováno v:
Archives of Pediatrics & Adolescent Medicine. 134:1095
Argininosuccinicaciduria is a rare genetic error of the Krebs-Henseleit urea cycle due to the absence or deficiency of the enzyme argininosuccinate lyase and is associated with mental retardation, seizures, ataxia, and hepatomegaly. Hyperammonemia ma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f8c48b1ba19896416b33ff3fecc4c1ac
https://doi.org/10.1001/archpedi.1980.02130230073023
https://doi.org/10.1001/archpedi.1980.02130230073023