Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 212

1.

Cognitive dysfunction as the major presenting feature of Becker's muscular dystrophy.

North KN, Miller G, Iannaccone ST, Clemens PR, Chad DA, Bella I, Smith TW, Beggs AH, Specht LA.

Neurology. 1996 Feb;46(2):461-5.

PMID:
8614513
2.

[Post exercise myalgias as presentation form of dystrophinopathy].

Kleinsteuber K, Rocco P, Herrera L, Vainzof M, Birke ME, Yáñez M, Flandes A, Zatz M, de Carvallo P, Avaria MA.

Rev Med Chil. 2000 Jul;128(7):772-7. Spanish.

PMID:
11050839
3.

[Limb-girdle syndrome. A study of 46 cases].

Ferrer X, Larrivière M, Coquet M, Ellie E, Lagueny A, Julien J.

Rev Neurol (Paris). 1993;149(12):788-93. Review. French.

PMID:
7997739
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.

Dystrophinopathy presenting as congenital muscular dystrophy.

Kyriakides T, Gabriel G, Drousiotou A, Meznanic-Petrusa M, Middleton L.

Neuromuscul Disord. 1994 Jul;4(4):387-92.

PMID:
7981596
6.

Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 3. Differential diagnosis and prognosis.

Nicholson LV, Johnson MA, Bushby KM, Gardner-Medwin D, Curtis A, Ginjaar IB, den Dunnen JT, Welch JL, Butler TJ, Bakker E, et al.

J Med Genet. 1993 Sep;30(9):745-51.

7.

Muscular dystrophy, mental retardation and cardiomyopathy not associated with dystrophin deficiency.

Villanova M, Malandrini A, Biancotti R, Löfgren A, Mongini T, Six J, Salvestroni R, Parrotta E, Van Broeckhoven C, Paolozzi C, Guazzi G.

Neuromuscul Disord. 1996 May;6(3):167-72.

PMID:
8784804
8.

Manifesting carriers of Xp21 muscular dystrophy; lack of correlation between dystrophin expression and clinical weakness.

Sewry CA, Sansome A, Clerk A, Sherratt TG, Hasson N, Rodillo E, Heckmatt JZ, Strong PN, Dubowitz V.

Neuromuscul Disord. 1993 Mar;3(2):141-8.

PMID:
8358239
9.

Distinction of Becker's muscular dystrophy from limb-girdle type by dystrophin analysis.

Jain S, Jha SK, Thomas M, Sarkar C, Maheshwari MC.

J Assoc Physicians India. 1994 Aug;42(8):624-5. No abstract available.

PMID:
7868558
10.

Undetectable dystrophin can still result in a relatively benign phenotype of dystrophinopathy.

Hattori N, Kaido M, Nishigaki T, Inui K, Fujimura H, Nishimura T, Naka T, Hazama T.

Neuromuscul Disord. 1999 Jun;9(4):220-6.

PMID:
10399748
11.

Becker muscular dystrophy or spinal muscular atrophy?--Dystrophin studies resolve conflicting results of electromyography and muscle biopsy.

McDonald TD, Medori R, Younger DS, Chang HW, Minetti C, Uncini A, Bonilla E, Hays AP, Lovelace RE.

Neuromuscul Disord. 1991;1(3):195-200.

PMID:
1822794
12.

Becker's muscular dystrophy aggravating facioscapulohumeral muscular dystrophy--double trouble as an explanation for an atypical phenotype.

Rudnik-Schöneborn S, Weis J, Kress W, Häusler M, Zerres K.

Neuromuscul Disord. 2008 Nov;18(11):881-5. doi: 10.1016/j.nmd.2008.06.387. Epub 2008 Aug 5.

PMID:
18684626
13.

[Application of combined DNA and dystrophin protein analysis in the diagnosis of Duchenne's and Becker's muscular dystrophy in 102 Dutch patients].

Ginjaar HB, Bakker E, Busch HF, Moorman AF, de Visser M, van Ommen JB.

Ned Tijdschr Geneeskd. 1993 Jan 9;137(2):68-75. Dutch.

PMID:
8421530
14.

[Becker's benign muscular dystrophy. Observations on 1 family].

Armocida G, Cottini R, Finavera L, Majeron MA.

Minerva Med. 1978 May 19;69(25):1745-8. Italian.

PMID:
662177
15.

Dystrophinopathy in isolated female patients with muscular dystrophy.

Serdaroglu A, Kotiloglu E, Caglar M, Topaloglu H.

Pediatr Pathol Lab Med. 1996 May-Jun;16(3):393-402.

PMID:
9025841
16.

Somatic mosaicism of a point mutation in the dystrophin gene in a patient presenting with an asymmetrical muscle weakness and contractures.

Helderman-van den Enden AT, Ginjaar HB, Kneppers AL, Bakker E, Breuning MH, de Visser M.

Neuromuscul Disord. 2003 May;13(4):317-21.

PMID:
12868501
17.

Asymptomatic dystrophinopathy.

Morrone A, Zammarchi E, Scacheri PC, Donati MA, Hoop RC, Servidei S, Galluzzi G, Hoffman EP.

Am J Med Genet. 1997 Mar 31;69(3):261-7.

PMID:
9096754
18.

Characterization of dystrophin in muscle-biopsy specimens from patients with Duchenne's or Becker's muscular dystrophy.

Hoffman EP, Fischbeck KH, Brown RH, Johnson M, Medori R, Loike JD, Harris JB, Waterston R, Brooke M, Specht L, et al.

N Engl J Med. 1988 May 26;318(21):1363-8.

PMID:
3285207
19.

[Symptomatic carriers of dystrophinopathy with chromosome X inactivation bias].

Lesca G, Demarquay G, Llense S, Streichenberger N, Petiot P, Michel-Calemard L, Récan D, Vial C, Ollagnon-Roman E.

Rev Neurol (Paris). 2003 Sep;159(8-9):775-80. French.

PMID:
13679720
20.

Dystrophinopathy in a young boy with Klinefelter's syndrome.

Santoro L, Pastore L, Rippa PG, Orsini AV, Del Giudice E, Vita G, Frisso G, Salvatore F.

Muscle Nerve. 1998 Jun;21(6):792-5.

PMID:
9585334

Supplemental Content

Support Center