Shapiro F - Search Results

1

Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management.

Bushby K, Finkel R, Birnkrant DJ, Case LE, Clemens PR, Cripe L, Kaul A, Kinnett K, McDonald C, Pandya S, Poysky J, Shapiro F, Tomezsko J, Constantin C; DMD Care Considerations Working Group. Bushby K, et al. Among authors: shapiro f. Lancet Neurol. 2010 Jan;9(1):77-93. doi: 10.1016/S1474-4422(09)70271-6. Epub 2009 Nov 27. Lancet Neurol. 2010. PMID: 19945913 Review.

2

Inefficient dystrophin expression after cord blood transplantation in Duchenne muscular dystrophy.

Kang PB, Lidov HG, White AJ, Mitchell M, Balasubramanian A, Estrella E, Bennett RR, Darras BT, Shapiro FD, Bambach BJ, Kurtzberg J, Gussoni E, Kunkel LM. Kang PB, et al. Muscle Nerve. 2010 Jun;41(6):746-50. doi: 10.1002/mus.21702. Muscle Nerve. 2010. PMID: 20513101 Free PMC article.

3

Association of Duchenne muscular dystrophy with autism spectrum disorder.

Wu JY, Kuban KC, Allred E, Shapiro F, Darras BT. Wu JY, et al. Among authors: shapiro f. J Child Neurol. 2005 Oct;20(10):790-5. doi: 10.1177/08830738050200100201. J Child Neurol. 2005. PMID: 16417872

4

Exploring the molecular basis for variability among patients with Becker muscular dystrophy: dystrophin gene and protein studies.

Beggs AH, Hoffman EP, Snyder JR, Arahata K, Specht L, Shapiro F, Angelini C, Sugita H, Kunkel LM. Beggs AH, et al. Among authors: shapiro f. Am J Hum Genet. 1991 Jul;49(1):54-67. Am J Hum Genet. 1991. PMID: 2063877 Free PMC article.

5

A mutation in the alpha 3 chain of type IX collagen causes autosomal dominant multiple epiphyseal dysplasia with mild myopathy.

Bönnemann CG, Cox GF, Shapiro F, Wu JJ, Feener CA, Thompson TG, Anthony DC, Eyre DR, Darras BT, Kunkel LM. Bönnemann CG, et al. Among authors: shapiro f. Proc Natl Acad Sci U S A. 2000 Feb 1;97(3):1212-7. doi: 10.1073/pnas.97.3.1212. Proc Natl Acad Sci U S A. 2000. PMID: 10655510 Free PMC article.

6

Posterior spinal fusion for scoliosis in duchenne muscular dystrophy diminishes the rate of respiratory decline.

Velasco MV, Colin AA, Zurakowski D, Darras BT, Shapiro F. Velasco MV, et al. Among authors: shapiro f. Spine (Phila Pa 1976). 2007 Feb 15;32(4):459-65. doi: 10.1097/01.brs.0000255062.94744.52. Spine (Phila Pa 1976). 2007. PMID: 17304138

7

Tranexamic acid diminishes intraoperative blood loss and transfusion in spinal fusions for duchenne muscular dystrophy scoliosis.

Shapiro F, Zurakowski D, Sethna NF. Shapiro F, et al. Spine (Phila Pa 1976). 2007 Sep 15;32(20):2278-83. doi: 10.1097/BRS.0b013e31814cf139. Spine (Phila Pa 1976). 2007. PMID: 17873823

8

Primary gamma-sarcoglycanopathy (LGMD 2C): broadening of the mutational spectrum guided by the immunohistochemical profile.

Bönnemann CG, Wong J, Jones KJ, Lidov HG, Feener CA, Shapiro F, Darras BT, Kunkel LM, North KN. Bönnemann CG, et al. Among authors: shapiro f. Neuromuscul Disord. 2002 Mar;12(3):273-80. doi: 10.1016/s0960-8966(01)00276-0. Neuromuscul Disord. 2002. PMID: 11801399

9

Progression of spinal deformity in wheelchair-dependent patients with Duchenne muscular dystrophy who are not treated with steroids: coronal plane (scoliosis) and sagittal plane (kyphosis, lordosis) deformity.

Shapiro F, Zurakowski D, Bui T, Darras BT. Shapiro F, et al. Bone Joint J. 2014 Jan;96-B(1):100-5. doi: 10.1302/0301-620X.96B1.32117. Bone Joint J. 2014. PMID: 24395319 Free article.

10

Prediction of dystrophin phenotype by DNA analysis in Duchenne/Becker muscular dystrophy.

Specht LA, Beggs AH, Korf B, Kunkel LM, Shapiro F. Specht LA, et al. Among authors: shapiro f. Pediatr Neurol. 1992 Nov-Dec;8(6):432-6. doi: 10.1016/0887-8994(92)90004-i. Pediatr Neurol. 1992. PMID: 1476571

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