240 related articles for article (PubMed ID: 28216480)
1. Co-incidence of Turner syndrome and Duchenne muscular dystrophy - an important problem for the clinician.
Kaczorowska E; Zimowski J; Cichoń-Kotek M; Mrozińska A; Purzycka J; Wierzba J; Limon J; Lipska-Ziętkiewicz BS
Dev Period Med; 2016; 20(4):273-278. PubMed ID: 28216480
[TBL] [Abstract][Full Text] [Related]
2. Turner Syndrome Mosaicism 45,X/46,XY with Genital Ambiguity and Duchenne Muscular Dystrophy: Translational Approach of a Rare Italian Case.
Lamanna B; Vinciguerra M; Dellino M; Cascella G; Cazzato G; Macorano E; Malvasi A; Scacco S; Cicinelli E; Loizzi V; Vimercati A; Cormio G; Paduano F; Cascardi E; Tatullo M
Int J Mol Sci; 2022 Nov; 23(22):. PubMed ID: 36430887
[TBL] [Abstract][Full Text] [Related]
3. Turner syndrome and Duchenne muscular dystrophy.
Verma S; Goyal P; Beam C; Shah D
Muscle Nerve; 2017 Aug; 56(2):E12-E15. PubMed ID: 28214339
[No Abstract] [Full Text] [Related]
4. DMD and West syndrome.
Cardas R; Iliescu C; Butoianu N; Seferian A; Gataullina S; Gargaun E; Nectoux J; Bienvenu T; Craiu D; Gidaro T; Servais L
Neuromuscul Disord; 2017 Oct; 27(10):911-913. PubMed ID: 28802771
[TBL] [Abstract][Full Text] [Related]
5. Duchenne muscular dystrophy in a female patient with a karyotype of 46,X,i(X)(q10).
Ou Z; Li S; Li Q; Chen X; Liu W; Sun X
Tohoku J Exp Med; 2010 Oct; 222(2):149-53. PubMed ID: 20944443
[TBL] [Abstract][Full Text] [Related]
6. Third case of Duchenne muscular dystrophy and West syndrome: Expanding the spectrum of the DMD neuropsychiatric phenotype.
Peña-Padilla C; Romero-Valenzuela I; Baldomero-López A; Sandoval-Talamantes AK; Castellanos-González A; Nagy PL; Kelly RR; Corona-Rivera JR
Neuromuscul Disord; 2021 May; 31(5):462-465. PubMed ID: 33741226
[TBL] [Abstract][Full Text] [Related]
7. 'Double trouble': diagnostic challenges in Duchenne muscular dystrophy in patients with an additional hereditary skeletal dysplasia.
Donkervoort S; Schindler A; Tesi-Rocha C; Schreiber A; Leach ME; Dastgir J; Hu Y; Mankodi A; Wagner KR; Friedman NR; Bönnemann CG
Neuromuscul Disord; 2013 Dec; 23(12):955-61. PubMed ID: 24070816
[TBL] [Abstract][Full Text] [Related]
8. Molecular characterization of co-occurring Duchenne muscular dystrophy and X-linked oculo-facio-cardio-dental syndrome in a girl.
Jiang YH; Fang P; Adesina AM; Furman P; Johnston JJ; Biesecker LG; Brown CW
Am J Med Genet A; 2009 Jun; 149A(6):1249-52. PubMed ID: 19449433
[TBL] [Abstract][Full Text] [Related]
9. 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. PubMed ID: 26718981
[TBL] [Abstract][Full Text] [Related]
10. Duchenne muscular dystrophy in a 4-year-old girl due to heterozygous frame shift deletion of the dystrophin gene and skewed X-inactivation.
Schänzer A; Rau I; Kress W; Köhler A; Neubauer B; Hahn A
Klin Padiatr; 2012 Jul; 224(4):256-8. PubMed ID: 22549471
[TBL] [Abstract][Full Text] [Related]
11. Novel mutation in exon 56 of the dystrophin gene in a child with Duchenne muscular dystrophy.
Zhu JF; Liu HH; Zhou T; Tian L
Int J Mol Med; 2013 Nov; 32(5):1166-70. PubMed ID: 24065205
[TBL] [Abstract][Full Text] [Related]
12. Screening of dystrophin gene deletions in Malaysian patients with Duchenne muscular dystrophy.
Marini M; Salmi AA; Watihayati MS; SMardziah MD; Zahri MK; Hoh BP; Ankathil R; Lai PS; Zilfalil BA
Med J Malaysia; 2008 Mar; 63(1):31-4. PubMed ID: 18935728
[TBL] [Abstract][Full Text] [Related]
13. Genetic diagnosis of Duchenne and Becker muscular dystrophy using multiplex ligation-dependent probe amplification in Rwandan patients.
Uwineza A; Hitayezu J; Murorunkwere S; Ndinkabandi J; Kalala Malu CK; Caberg JH; Dideberg V; Bours V; Mutesa L
J Trop Pediatr; 2014 Apr; 60(2):112-7. PubMed ID: 24213305
[TBL] [Abstract][Full Text] [Related]
14. Genetics and emerging treatments for Duchenne and Becker muscular dystrophy.
Wein N; Alfano L; Flanigan KM
Pediatr Clin North Am; 2015 Jun; 62(3):723-42. PubMed ID: 26022172
[TBL] [Abstract][Full Text] [Related]
15. Duchenne Muscular Dystrophy: A Practice Update.
Suthar R; Sankhyan N
Indian J Pediatr; 2018 Apr; 85(4):276-281. PubMed ID: 28653137
[TBL] [Abstract][Full Text] [Related]
16. Becker muscular dystrophy with r(X) carrying an out-of-frame DMD deletion.
Lee KA; Han SH; Choi JR; Chung JS; Choi YC
Pediatr Neurol; 2008 Aug; 39(2):129-32. PubMed ID: 18639760
[TBL] [Abstract][Full Text] [Related]
17. Coinheritance of Noonan syndrome and Becker muscular dystrophy.
Dinopoulos A; Papadopoulou A; Manta P; Kekou K; Kanelopoulos T; Fretzayas A; Kitsiou S
Neuromuscul Disord; 2010 Jan; 20(1):61-3. PubMed ID: 19875288
[TBL] [Abstract][Full Text] [Related]
18. Prenatal diagnosis of DMD in a female foetus affected by Turner syndrome.
Satre V; Monnier N; Devillard F; Amblard F; Lunardi J
Prenat Diagn; 2004 Nov; 24(11):913-7. PubMed ID: 15565644
[TBL] [Abstract][Full Text] [Related]
19. Novel human pathological mutations. Gene symbol: DMD. Disease: Muscular Dystrophy, Duchenne.
Dasouki M; Barohn R; Hegde M
Hum Genet; 2010 Jan; 127(1):109. PubMed ID: 20108418
[No Abstract] [Full Text] [Related]
20. Frameshift deletion mechanisms in Egyptian Duchenne and Becker muscular dystrophy families.
Elhawary NA; Shawky RM; Hashem N
Mol Cells; 2004 Oct; 18(2):141-9. PubMed ID: 15528988
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]