9 DYSLIPIDEMIA AS A FACTOR FOR PROGRESSION OF RENAL OSTEODYSTROPHY AND CORONARY HEART DISEASE IN PATIENTS WITH CHRONIC KIDNEY DISEASE ON PERITONEAL DIALYSIS

10 Amelioration of intracellular Ca regulation by exon-45 skipping in Duchenne muscular dystrophy-induced pluripotent stem cell-derived cardiomyocytes.

11 Intraocular lens power prediction for triple procedures in Fuchs' dystrophy using multiple regression analysis.

12 Assessment of 6 STR loci for prenatal diagnosis of Duchenne Muscular Dystrophy.

13 Research advances in limb-girdle muscular dystrophy type 2Q

14 Rapid prenatal diagnosis of Facioscapulohumeral Muscular Dystrophy 1 by combined Bionano optical mapping and karyomapping.

15 Downregulation of the NLRP3 inflammasome by adiponectin rescues Duchenne muscular dystrophy

16 European lipodystrophy registry: background and structure.

17 Morning myopic shift and glare in advanced Fuchs endothelial corneal dystrophy.

18 Is leukodystrophy really a feature of PIGT-CDG?

19 Small-molecule activation of lysosomal TRP channels ameliorates Duchenne muscular dystrophy in mouse models.

20 Laminin and Integrin in LAMA2-Related Congenital Muscular Dystrophy: From Disease to Therapeutics.

21 Dysregulation of Calcium Handling in Duchenne Muscular Dystrophy-Associated Dilated Cardiomyopathy: Mechanisms and Experimental Therapeutic Strategies.

22 Human Galectin-1 Improves Sarcolemma Stability and Muscle Vascularization in the mdx Mouse Model of Duchenne Muscular Dystrophy

23 Expression of dystrophin -glycoprotein complex at the skeletal muscle sarcolemma in Duchenne muscular dystrophy

24 Ultra-structural time-course study in the C. elegans model for Duchenne muscular dystrophy highlights a crucial role for sarcomere-anchoring structures and sarcolemma integrity in the earliest steps of the muscle degeneration process

25 The intracellular Ca<sup>2+</sup> channel MCOLN1 is required for sarcolemma repair to prevent muscular dystrophy

26 Development of a high-throughput screen to identify small molecule enhancers of sarcospan for the treatment of Duchenne muscular dystrophy

27 Moderate exercise improves function and increases adiponectin in the mdx mouse model of muscular dystrophy

28 Combined deletions of and cause chondrodystrophy and embryonic lethality in the Creeper chicken.

29 Sequence Variants in Three Genes Underlying Leukodystrophy in Pakistani Families.

30 [Prenatal dystrophy]

31 Ultrastructure of peripheral nerve in metachromatic leucodystrophy

32 Juvenile metachromatic leucodystrophy

33 Electron microscopic study of metachromatic leucodystrophy

34 [Prenatal dystrophy].

35 Skeletal muscle pathology in ovine congenital progressive muscular dystrophy

36 Dietary Habits and Their Association with Metabolic Abnormalities in Human Immunodeficiency Virus—Related Lipodystrophy

37 Distal infantile neuroaxonal dystrophy – a new familial variant with perineuronal argyrophilic bodies

38 Decrease of neurons in the medullary arcuate nucleus in myotonic dystrophy

39 Exclusive association and simultaneous appearance of congophilic plaques and AT8-positive dystrophic neurites in Tg2576 mice suggest a mechanism of senile plaque formation and progression of neuritic dystrophy in Alzheimer’s disease

40 infrared imaging enhances retinal crystals in bietti’s crystalline dystrophy

41 frequency of mixed onychomycosis with total nail dystrophy in patients attended in a guatemalan dermatology center

42 desflurane anaesthesia in myotonic dystrophy

43 fat embolism after fractures in duchenne muscular dystrophy: an underdiagnosed complication? a systematic review

44 duchenne muscular dystrophy: overview and future challenges

45 pneumothoraces in collagen vi-related dystrophy: a case series and recommendations for management

46 lasik in selected patients with posterior polymorphous corneal dystrophy

47 platelet-rich autoplasma in surgical treatment of degenerative dystrophyc tendomuscular lesions

48 relationship between neuropsychological impairment and grey and white matter changes in adult-onset myotonic dystrophy type 1

49 cellular transplantation alters the disease progression in becker’s muscular dystrophy

50 current challenges and future directions in recombinant aav-mediated gene therapy of duchenne muscular dystrophy

51 cerebral x-linked adrenoleukodystrophy: follow-up with magnetic resonance imaging adrenoleucodistrofia ligada ao x: acompanhamento por ressonância magnética

52 avaliação dos resultados da artrodese da articulação escapulotorácica no tratamento da escápula alada na distrofia fascioescapulumeral evaluation of scapulothoracic arthrodesis results in the treatment of winged scapula in facioscapulohumeral dystrophy

53 body fat distribution in women with familial partial lipodystrophy caused by mutation in the lamin a/c gene

54 living with severe physical impairment, duchenne's muscular dystrophy and home mechanical ventilation

55 two cases of endometrial cancer in twin sisters with myotonic dystrophy

56 congenital lipodystrophy with defective leucocyte function (a case report).

57 role of mitochondria in hiv infection and associated metabolic disorders: focus on nonalcoholic fatty liver disease and lipodystrophy syndrome

58 overview of hiv-related lipodystrophy

59 treatment of sleep central apnea with non-invasive mechanical ventilation with 2 levels of positive pressure (bilevel) in a patient with myotonic dystrophy type 1

60 therapeutic potential of matrix metalloproteinases in duchenne muscular dystrophy

61 lichen striatus with onychodystrophy in an infant

62 serum creatinine distinguishes duchenne muscular dystrophy from becker muscular dystrophy in patients aged ≤3 years: a retrospective study

63 a retrospective study of the association between fuchs’ endothelial dystrophy and glaucoma

64 a selective detection of lysophosphatidylcholine in dried blood spots for diagnosis of adrenoleukodystrophy by lc-ms/ms

65 relationship of white and gray matter abnormalities to clinical and genetic features in myotonic dystrophy type 1

66 chronic administration of a leupeptin-derived calpain inhibitor fails to ameliorate severe muscle pathology in a canine model of duchenne muscular dystrophy

67 echocardiographic image quality deteriorates with age in children and young adults with duchenne muscular dystrophy

68 análise da expressão do colágeno vi na distrofia muscular congênita analysis of the expression of collagen vi in congenital muscular dystrophy

69 cardiac involvement in myotonic dystrophy

70 microperimetric evaluation in patients with adult-onset foveomacular vitelliform dystrophy

71 quantitative ultrasound: measurement considerations for the assessment of muscular dystrophy and sarcopenia

72 stem cell-transplantation therapy for adrenoleukodystrophy: current perspectives

73 anestesia em paciente portador de distrofia muscular de duchenne: relato de casos anestesia en un paciente portador de distrofia muscular de duchenne: relato de casos anesthesia for duchenne muscular dystrophy patients: case reports

74 distrofia muscular nutricional em ovinos na paraíba nutritional muscular dystrophy in sheep in paraíba

75 Suppression of the C/EBP family of transcription factors in adipose tissue causes lipodystrophy

76 Turnover of Adipose Components and Mitochondrial DNA in Humans: Kinetic Biomarkers for Human Immunodeficiency Virus—Associated Lipodystrophy and Mitochondrial Toxicity?

77 Studies of Adipose Tissue Metabolism in Human Immunodeficiency Virus—Associated Lipodystrophy

78 Retrospective evaluation of patients with X-linked adrenoleukodystrophy with a wide range of clinical presentations: a single center experience

79 Insulin resistance and diabetes mellitus in transgenic mice expressing nuclear SREBP-1c in adipose tissue: model for congenital generalized lipodystrophy

80 [Asphyxiating thoracic dystrophy (Jeune syndrome). Description of a clinical case]

81 Mutations in proteasome subunit β type 8 cause chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature with evidence of genetic and phenotypic heterogeneity

82 [Asphyxiating thoracic dystrophy (Jeune syndrome). Description of a clinical case].

83 Imaging the Corneal Endothelium in Fuchs Corneal Endothelial Dystrophy

84 The administration of antisense oligonucleotide golodirsen reduces pathological regeneration in patients with Duchenne muscular dystrophy

85 Membrane repair defects in muscular dystrophy are linked to altered interaction between MG53, caveolin-3, and dysferlin

86 Insulin resistance and diabetes mellitus in transgenic mice expressing nuclear SREBP-1c in adipose tissue: model for congenital generalized lipodystrophy

87 Safety and efficacy of givinostat in boys with Duchenne muscular dystrophy (EPIDYS): a multicentre, randomised, double-blind, placebo-controlled, phase 3 trial.

88 T1-Mapping and extracellular volume estimates in pediatric subjects with Duchenne muscular dystrophy and healthy controls at 3T

89 Association Between Myocardial Oxygenation and Fibrosis in Duchenne Muscular Dystrophy: Analysis by Rest Oxygenation-Sensitive Magnetic Resonance Imaging.

90 PSYCHOLOGICAL FEATURES OF THE SUBJECTIVE PERCEPTION OF THE QUALITY OF LIFE OF PATIENTS WITH HEPATOCEREBRAL DYSTROPHY.

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