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51. Genotype-Phenotype studies of VCP-associated Inclusion Body Myopathy with Paget Disease of Bone and/or Frontotemporal Dementia

52. Radiological features of Paget disease of bone associated with VCP myopathy

53. The Multiple Faces of Valosin-Containing Protein-Associated Diseases: Inclusion Body Myopathy with Paget’s Disease of Bone, Frontotemporal Dementia, and Amyotrophic Lateral Sclerosis

55. Unique Capabilities of Genome Sequencing for Rare Disease Diagnosis

56. A comprehensive study of skeletal muscle imaging in FHL1‐related reducing body myopathy

57. Common and variable clinical, histological, and imaging findings of recessive RYR1-related centronuclear myopathy patients

60. Upper extremity outcome measures for collagen VI-related myopathy and LAMA2-related muscular dystrophy

62. Recurrent de-novo gain-of-function mutation in SPTLC2 confirms dysregulated sphingolipid production to cause juvenile amyotrophic lateral sclerosis.

63. Recurrent de novo SPTLC2 variant causes childhoodonset amyotrophic lateral sclerosis (ALS) by excess sphingolipid synthesis.

64. Longitudinal changes in clinical outcome measures in COL6-related dystrophies and LAMA2-related dystrophies

65. Clinical, genetic, and pathologic characterization of FKRP Mexican founder mutation c.1387A>G

67. Bi-allelic variants in HMGCR cause an autosomal-recessive progressive limb-girdle muscular dystrophy

68. Unusually severe muscular dystrophy upon in-frame deletion of the dystrophin rod domain and lack of compensation by membrane-localized utrophin

69. Pathogenic variants in TNNC2 cause congenital myopathy due to an impaired force response to calcium

70. Recurrent de-novo gain-of-functionmutation in SPTLC2confirms dysregulated sphingolipid production to cause juvenile amyotrophic lateral sclerosis

71. Recurrent de novo SPTLC2variant causes childhood-onset amyotrophic lateral sclerosis (ALS) by excess sphingolipid synthesis

72. Anti-HMGCR myopathy may resemble limb-girdle muscular dystrophy

73. Recessive mutations in muscle-specific isoforms of FXR1 cause congenital multi-minicore myopathy

74. Clinical Manifestation of Nebulin-Associated Nemaline Myopathy

75. Electrophysiological Characterization of aMYH7Variant With Tremor Phenotype

76. P452: Specifying the ACMG/AMP variant sequence interpretation guidelines for congenital myopathies*

77. Results of a two-year pilot study of clinical outcome measures in collagen VI- and laminin alpha2-related congenital muscular dystrophies

78. Detection of colon cancer recurrences during follow-up care by general practitioners versus surgeons

79. Dihydropyridine receptor (DHPR, CACNA1S) congenital myopathy

80. English Cross-Cultural Translation and Validation of the Neuromuscular Score: A System for Motor Function Classification in Patients With Neuromuscular Diseases

81. Electrical impedance myography in individuals with collagen 6 and laminin α‐2 congenital muscular dystrophy: a cross‐sectional and 2‐year analysis

82. Loss of tubulin deglutamylase CCP1 causes infantile‐onset neurodegeneration

85. The SPTLC1 p.S331 mutation bridges sensory neuropathy and motor neuron disease and has implications for treatment

87. Novel SNP array analysis and exome sequencing detect a homozygous exon 7 deletion of MEGF10 causing early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD)

88. Antibiotic prophylaxis for acute cholecystectomy: PEANUTS II multicentre randomized non-inferiority clinical trial

92. Electrophysiological Characterization of a MYH7 Variant with Tremor Phenotype.

94. Recognizable Pattern of Arthrogryposis and Congenital Myopathy Caused by the Recurrent TTN Metatranscript-only c.39974-11T > G Splice Variant

95. FXR1-related congenital myopathy: expansion of the clinical and genetic spectrum

96. Biallelic variants in TAMM41 are associated with low muscle cardiolipin levels, leading to neonatal mitochondrial disease

97. A complex COL6A3 mutation identification: it takes an international village

98. Antibiotic prophylaxis for acute cholecystectomy: PEANUTS II multicentre randomized non-inferiority clinical trial

100. Mutation-Specific Effects on Thin Filament Length in Thin Filament Myopathy

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