Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 82

1.

[Clinical and pathological features of 50 children with Duchenne's muscular dystrophy].

Li QX, Yang H, Zhang N, Xiao B, Bi FF, Li J.

Zhongguo Dang Dai Er Ke Za Zhi. 2012 Oct;14(10):746-50. Chinese.

2.

Utility of dystrophin and utrophin staining in childhood muscular dystrophy.

Sundaram C, Vydehi B, Meena K, Murthy J.

Indian J Pathol Microbiol. 2004 Jul;47(3):367-9.

PMID:
16295426
4.

Absence of neuronal nitric oxide synthase (nNOS) as a pathological marker for the diagnosis of Becker muscular dystrophy with rod domain deletions.

Torelli S, Brown SC, Jimenez-Mallebrera C, Feng L, Muntoni F, Sewry CA.

Neuropathol Appl Neurobiol. 2004 Oct;30(5):540-5.

PMID:
15488030
5.

[Association between dystrophin and neuronal nitric oxide synthase in muscles of progressive muscular dystrophy].

Wang S, Shen D.

Zhonghua Yi Xue Za Zhi. 2002 Feb 10;82(3):155-7. Chinese.

PMID:
11953148
6.

Duchenne and Becker muscular dystrophy: a molecular and immunohistochemical approach.

Freund AA, Scola RH, Arndt RC, Lorenzoni PJ, Kay CK, Werneck LC.

Arq Neuropsiquiatr. 2007 Mar;65(1):73-6.

7.

Dystrophinopathies in females.

Hausmanowa-Petrusewicz I, Fidziańska A, Niebrój-Dobosz I, Dorobek M, Bojakowski J.

Folia Neuropathol. 2000;38(1):7-12.

PMID:
11057028
8.

Endomysial fibrosis in Duchenne muscular dystrophy: a marker of poor outcome associated with macrophage alternative activation.

Desguerre I, Mayer M, Leturcq F, Barbet JP, Gherardi RK, Christov C.

J Neuropathol Exp Neurol. 2009 Jul;68(7):762-73. doi: 10.1097/NEN.0b013e3181aa31c2.

PMID:
19535995
9.

Duchenne muscular dystrophy: a clinical, histopathological and genetic study at a neurology tertiary care center in Southern India.

Swaminathan B, Shubha GN, Shubha D, Murthy AR, Kiran Kumar HB, Shylashree S, Gayathri N, Jamuna R, Jain S, Purushottam M, Nalini A.

Neurol India. 2009 Nov-Dec;57(6):734-8. doi: 10.4103/0028-3886.59468.

10.

Changes in skeletal muscle expression of AQP1 and AQP4 in dystrophinopathy and dysferlinopathy patients.

Au CG, Butler TL, Egan JR, Cooper ST, Lo HP, Compton AG, North KN, Winlaw DS.

Acta Neuropathol. 2008 Sep;116(3):235-46. doi: 10.1007/s00401-008-0369-z. Epub 2008 Apr 8.

PMID:
18392839
11.

Increased dysferlin expression in Duchenne muscular dystrophy.

Vontzalidis A, Terzis G, Manta P.

Anal Quant Cytopathol Histpathol. 2014 Feb;36(1):15-22.

PMID:
24902367
12.

Systemic administration of PRO051 in Duchenne's muscular dystrophy.

Goemans NM, Tulinius M, van den Akker JT, Burm BE, Ekhart PF, Heuvelmans N, Holling T, Janson AA, Platenburg GJ, Sipkens JA, Sitsen JM, Aartsma-Rus A, van Ommen GJ, Buyse G, Darin N, Verschuuren JJ, Campion GV, de Kimpe SJ, van Deutekom JC.

N Engl J Med. 2011 Apr 21;364(16):1513-22. doi: 10.1056/NEJMoa1011367. Epub 2011 Mar 23. Erratum in: N Engl J Med. 2011 Oct 6;365(14):1361.

13.

Dystrophin analysis in carriers of Duchenne and Becker muscular dystrophy.

Hoogerwaard EM, Ginjaar IB, Bakker E, de Visser M.

Neurology. 2005 Dec 27;65(12):1984-6.

PMID:
16380627
14.

[Sibling brother and sister both with Duchenne muscular dystrophy].

Zhang YN, Zhang C, Feng HY, Sun XF, Lu XL, Li SY, Zhang HM, Li MS, Yu MJ, Wang SH, Huang H, Li Z, Shen BC.

Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2007 Aug;29(4):543-7. Chinese.

15.

[Clinical pathologic studies and genetic analysis of a female Duchenne muscular dystrophy family].

Feng HY, Zhang C, Li Z, Yao XL, Zeng Y.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Feb;22(1):65-7. Chinese.

PMID:
15696483
16.

Genetic and Early Clinical Manifestations of Females Heterozygous for Duchenne/Becker Muscular Dystrophy.

Papa R, Madia F, Bartolomeo D, Trucco F, Pedemonte M, Traverso M, Broda P, Bruno C, Zara F, Minetti C, Fiorillo C.

Pediatr Neurol. 2016 Feb;55:58-63. doi: 10.1016/j.pediatrneurol.2015.11.004. Epub 2015 Nov 26.

PMID:
26718981
17.
18.

9 year old girl with progressive weakness.

Seemann N, Campbell C, Hammond R, Prasad C.

Brain Pathol. 2010 Jan;20(1):255-6. doi: 10.1111/j.1750-3639.2009.00344.x.

PMID:
20438484
19.

[Therapy of Duchenne muscular dystrophy with umbilical cord blood stem cell transplantation].

Zhang C, Feng HY, Huang SL, Fang JP, Xiao LL, Yao XL, Chen C, Ye X, Zeng Y, Lu XL, Wen JM, Zhang WX, Li Z, Feng SW, Xu HG, Huang K, Zhou DH, Chen W, Xie YM, Xi J, Zhang M, Li Y, Liu Y.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Aug;22(4):399-405. Chinese.

PMID:
16086277
20.

Genetic polymorphism in muscle biopsies of Duchenne and Becker muscular dystrophy patients.

Anand A, Prabhakar S, Kaul D.

Neurol India. 1999 Sep;47(3):218-23.

Supplemental Content

Support Center