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Items: 1 to 20 of 96

1.

Apparent diffusion coefficient vale of the brain in patients with Gaucher's disease type II and type III.

Abdel Razek AA, Abd El-Gaber N, Abdalla A, Fathy A, Azab A, Rahman AA.

Neuroradiology. 2009 Nov;51(11):773-9. doi: 10.1007/s00234-009-0548-1. Epub 2009 Jul 15.

PMID:
19603156
2.

Apparent diffusion coefficient of the vertebral bone marrow in children with Gaucher's disease type I and III.

Razek AA, Abdalla A, Fathy A, Megahed A.

Skeletal Radiol. 2013 Feb;42(2):283-7. doi: 10.1007/s00256-012-1464-8. Epub 2012 Jun 21.

PMID:
22718272
3.

Proton MR Spectroscopy of the brain in children with neuronopathic Gaucher's disease.

Razek AA, Abdalla A, Gaber NA, Fathy A, Megahed A, Barakat T, Latif Alsayed MA.

Eur Radiol. 2013 Nov;23(11):3005-11. doi: 10.1007/s00330-013-2924-9. Epub 2013 Jun 20.

PMID:
23783781
4.

Subarachnoid hemorrhage in the subacute stage: elevated apparent diffusion coefficient in normal-appearing brain tissue after treatment.

Liu Y, Soppi V, Mustonen T, Könönen M, Koivisto T, Koskela A, Rinne J, Vanninen RL.

Radiology. 2007 Feb;242(2):518-25. Epub 2006 Dec 19.

PMID:
17179395
5.

Assessment of the liver and spleen in children with Gaucher's disease type I with diffusion-weighted MR imaging.

Razek AA, Abdalla A, Barakat T, El-Taher H, Ali K.

Blood Cells Mol Dis. 2016 Dec 20. pii: S1079-9796(16)30312-6. doi: 10.1016/j.bcmd.2016.12.004. [Epub ahead of print]

PMID:
28012701
6.

Type I Gaucher's disease with homozygous R463C mutation without neurological involvement.

Bolaman Z, Kadikoylu G, Levi E, Barutca S, Temucin K.

Haematologia (Budap). 2002;32(4):487-93.

PMID:
12803123
7.

A mutation in the human glucocerebrosidase gene in neuronopathic Gaucher's disease.

Tsuji S, Choudary PV, Martin BM, Stubblefield BK, Mayor JA, Barranger JA, Ginns EI.

N Engl J Med. 1987 Mar 5;316(10):570-5.

PMID:
2880291
8.

Novel frameshift mutation (Pro171fsX21) in neonatal type 2 Gaucher's disease.

Park HW, Lee Y, Kim GH, Lee BS, Kim KS, Yoo HW, Kim EA.

Gene. 2012 Oct 10;507(2):170-3. doi: 10.1016/j.gene.2012.06.090. Epub 2012 Jul 5.

PMID:
22772462
9.

Assessment of white matter integrity of autistic preschool children with diffusion weighted MR imaging.

Abdel Razek A, Mazroa J, Baz H.

Brain Dev. 2014 Jan;36(1):28-34. doi: 10.1016/j.braindev.2013.01.003. Epub 2013 Feb 8.

PMID:
23398955
10.

A diffusion-weighted template for gestational age-related apparent diffusion coefficient values in the developing fetal brain.

Cannie M, De Keyzer F, Meersschaert J, Jani J, Lewi L, Deprest J, Dymarkowski S, Demaerel P.

Ultrasound Obstet Gynecol. 2007 Sep;30(3):318-24.

11.

Prediction of severity of Gaucher's disease by identification of mutations at DNA level.

Zimran A, Sorge J, Gross E, Kubitz M, West C, Beutler E.

Lancet. 1989 Aug 12;2(8659):349-52.

PMID:
2569551
12.

[Gaucher's disease: clinical picture in 11 children].

Franco-Ornelas S, González-Vite M, Núñez-Villegas N, Solís-Labastida K, Brito-Trejo JM.

Rev Med Inst Mex Seguro Soc. 2012 Jan-Feb;50(1):107-12. Spanish.

PMID:
22768827
13.

Gaucher's disease: identification of novel mutant alleles and genotype-phenotype relationships.

Zhao H, Keddache M, Bailey L, Arnold G, Grabowski G.

Clin Genet. 2003 Jul;64(1):57-64.

PMID:
12791040
14.

Diffusion weighted MR findings of brain involvement in tuberous sclerosis.

Firat AK, Karakaş HM, Erdem G, Yakinci C, Biçak U.

Diagn Interv Radiol. 2006 Jun;12(2):57-60.

15.
16.

Oculomotor apraxia in a case of Gaucher's disease with homozygous T1448C mutation.

Tsai LP, Sue WC, Hwu WL, Lin KH, Wang TR.

Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1996 Jan-Feb;37(1):52-5.

PMID:
8936012
17.

Homozygous loss of a cysteine residue in the glucocerebrosidase gene results in Gaucher's disease with a hydropic phenotype.

Church HJ, Cooper A, Stewart F, Thornton CM, Wraith JE.

Eur J Hum Genet. 2004 Nov;12(11):975-8.

18.

Diffusion-weighted MR of the brain: methodology and clinical application.

Mascalchi M, Filippi M, Floris R, Fonda C, Gasparotti R, Villari N.

Radiol Med. 2005 Mar;109(3):155-97. Review. English, Italian.

PMID:
15775887
19.
20.

The glucocerebrosidase locus in Gaucher's disease: molecular analysis of a lysosomal enzyme.

Mistry PK, Cox TM.

J Med Genet. 1993 Nov;30(11):889-94. Review. No abstract available.

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