«LEUKODYSTROPHY» தொடர்புடைய ஆங்கிலம் புத்தகங்கள்
பின்வரும் புத்தக விவரத்தொகுப்புத் தேர்ந்தெடுப்பில்
leukodystrophy இன் பயன்பாட்டைக் கண்டறியுங்கள்.
leukodystrophy தொடர்பான புத்தகங்கள் மற்றும் ஆங்கிலம் இலக்கியத்தில் அதன் பயன்பாட்டுச் சூழலை வழங்குவதற்கு அதிலிருந்து பெறப்பட்ட சுருக்கமான சாரங்களைத் தொடர்புபடுத்துகின்றன.
1
Diag. Radiology Ped. Imaging
MR imaging is highly sensitive in determining the presence and assessing the
severity of underlying white matter abnormalities in patients with leukodystrophy.
Although the findings are often non specific, systematic analysis of the finer
details ...
2
Inborn Metabolic Diseases: Diagnosis and Treatment
Berger J, Loschl B, Bernheimer H et al (1997) Occurrence, distribution, and
phenotype of arylsulfatase A mutations in patients with metachromatic
leukodystrophy. Am J Med Genet 69:335- 76. 340 56. Rafi MA, Coppola S, Liu SL
et al (2003) ...
John Fernandes, Jean-Marie Saudubray, Georges van den Berghe, 2006
3
Atlas of Metabolic Diseases Second edition
Late-presenting metachromatic leukodystrophy. Lancet1996;348:1382. Furst W,
Sandhoff K. Activator proteins and topology of lysosomal sphingolipid catabolism.
Biochim BiophysActa1992;1126:1. Wu C-SC, Lee NM, Loh HH, etal.
William L Nyhan, Bruce A Barshop, Pinar T. Ozand, 2005
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The Molecular and Genetic Basis of Neurologic and ...
allele compound the difficulties in patients and earners of metachroma accurately
identifying tic leukodystrophy. Mol Genet Metab. 2003:79:83-90. Regis S,
Corsolini F, Stroppiano M] et al. Contribution of arylsulfatase A mutations located
bn ...
Please note that the content of this book primarily consists of articles available from Wikipedia or other free sources online. Leukodystrophy refers to a group of disorders characterized by dysfunction of the of the brain.
Frederic P Miller, Agnes F Vandome, John McBrewster, 2012
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Secondary Schizophrenia
Metachromatic leukodystrophy. In The Metabolic Basis of Inherited Disease,
Scriver C.R., BeaudetA.L., SlyW.S., etal. (Eds.). Eighth Ed., vol 3. New York:
McGraw-Hill, pp. 3695–724. 2. Hyde T. M., Ziegler J. C., Weinberger D. R.
Psychiatric ...
Perminder S. Sachdev, Matcheri S. Keshavan, 2010
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Individualized Healthcare Plans for the School Nurse: ...
Recurrent seizures in metachromatic leukodystrophy. Pediatric Neurology, 17(2),
150—154 Gieselmann, V., Kreysing, J., 86 von Figura, K. (1994). Genetics of
metachromatic leukodystrophy. Gene Therapy, 1(Suppl. 1), S87. Kaye, E. M. (
2001) ...
Cynthia K. Silkworth, 2005
8
Emery and Rimoin's Principles and Practice of Medical Genetics
P426L in the ARSA Gene: Prevalence in Metachromatic Leukodystrophy Patients
from European Countries. Mol. Genet. Metab. 2005, 86 (3), 353—359. Rauschka,
H.; Colsch, B.; Baumann, N.; Wevers, R.; Schmidbauer, M.; Krammer, M., et al.
David L. Rimoin, Reed E. Pyeritz, Bruce Korf, 2013
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Pediatric Neurology, Part III: Handbook of Clinical Neurology
Hematopoietic stem cell gene therapy in Hurler syndrome, globoid cell
leukodystrophy, metachromatic leukodystrophy and X-adrenoleukodystrophy.
Curr Opin Mol Ther 10: 471–478. Deconinck N, Messaaoui A, Ziereisen F et al. (
2008).
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Genetic Disorders and the Fetus: Diagnosis, Prevention and ...
V. The nature and significance of low sulfatase activity: a controlled study of brain
, liver and kidney in four patients with metachromatic leukodystrophy (MLD). Arch
Neurol 1965;13:593. 222. Jatzkewitz H, Mehl E. Cerebroside-sulphatase and ...
Aubrey Milunsky, Jeff Milunsky, 2011
«LEUKODYSTROPHY» வார்த்தையைக் கொண்டுள்ள புதிய உருப்படிகள்
பின்வரும் செய்தி உருப்படிகளின் சூழலில்
leukodystrophy என்ற வார்த்தையைப் பயன்படுத்துவது பற்றியும் எப்படிப் பயன்படுத்துவது என்பதைப் பற்றியும் தேசிய மற்றும் பன்னாட்டு அச்சகங்கள் என்ன பேசியிருக்கின்றன என்பதைக் கண்டறியுங்கள்.
Hope runs high at Rock the Park as clinical trials near
... is hoping to use the Team 2018 initiative to fund clinical trials that could lead to a cure for the infantile form of metachromatic leukodystrophy. «London Community News, ஜூலை 15»
New Products Posted to GenomeWeb
Transgenomics has launched the Leukodystrophy NGS Panel, which is designed to diagnose individuals with any of the roughly 40 inherited nervous system ... «GenomeWeb, ஜூலை 15»
Transgenomic Launches Most Comprehensive Test for Diagnosis of …
Tuesday morning, TBIO announced the launch of the most comprehensive genetic test for diagnosis of leukodystrophy. Leukodystrophy is a ... «Baystreet.ca, ஜூலை 15»
The Choice Life: National MLD conference brings support in numbers
She hadn't realized that there were so many other families who were struggling with Metachromatic Leukodystrophy (MLD). Feeling isolated ... «Daily Herald, ஜூலை 15»
Sprint Corporation (NYSE:S) Leading Top Gainers with Fitbit Inc …
... the diagnosis of leukodystrophy, a group of rare progressive genetic disorders. Transgenomic added that as the most comprehensive test on ... «StreetWise Report, ஜூலை 15»
New Roundup- Mylan N.V. (NASDAQ:MYL), Johnson & Johnson …
Transgenomic Inc. (NASDAQ:TBIO) released of Transgenomic Leukodystrophy NGS Panel for the diagnosis of leukodystrophy, a group of ... «StreetWise Report, ஜூலை 15»
Transgenomic (TBIO) Launches Genetic Test for Diagnosis of …
With the advent of improved genetic testing methods, the Global Leukodystrophy Initiative (GLIA) Consortium has issued diagnostic guidelines ... «StreetInsider.com, ஜூலை 15»
Closing Update: Stocks Climb For A Fourth Day, Extending Broad …
(+) TBIO, Launches genetic test to diagnose leukodystrophy, a group of rare, progressive genetic disorders that disrupt the growth and ... «Nasdaq, ஜூலை 15»
Health Care Sector Update for 07/14/2015: EYEG,OCUL,TNXP
(+) TBIO, Launches genetic test to diagnose leukodystrophy, a group of rare, progressive genetic disorders that disrupt the growth and ... «Nasdaq, ஜூலை 15»
Unusual 11 Mid-Day Movers 7/14: (TBIO) (BAMM) (EPRS) Higher …
Transgenomic, Inc. (Nasdaq: TBIO) 34.3% HIGHER; announced the launch of theTransgenomic Leukodystrophy NGS Panel for the diagnosis ... «StreetInsider.com, ஜூலை 15»
இல் உள்ள வார்த்தைகளில் மறைக்கப்பட்டிருக்கும் எல்லாவற்றையும் கண்டறியுங்கள் 
