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101. Efficacy of Omaveloxolone in Friedreich's Ataxia: Delayed‐Start Analysis of the MOXIe Extension.

104. Differentiating Profiles of Speech Impairments in Friedreich's Ataxia: A Perceptual and Instrumental Approach

108. Correspondence on “Screening for autosomal recessive and X-linked conditions during pregnancy and preconception: a practice resource of the American College of Medical Genetics and Genomics (ACMG)” by Gregg et al

115. An open-label trial in Friedreich ataxia suggests clinical benefit with high-dose resveratrol, without effect on frataxin levels

118. Correction: Reproductive genetic carrier screening for cystic fibrosis, fragile X syndrome, and spinal muscular atrophy in Australia: outcomes of 12,000 tests

120. The Responsiveness of Gait and Balance Outcomes to Disease Progression in Friedreich Ataxia

123. Lessons learnt from multifaceted diagnostic approaches to the first 150 families in Victoria’s Undiagnosed Diseases Program

125. Voice in Friedreich Ataxia

127. A family study implicates GBE1 in the etiology of autism spectrum disorder

129. Paternal retraction of a fragile X allele to normal size, showing normal function over two generations

137. Familial cortical dysplasia caused by mutation in the mammalian target of rapamycin regulator NPRL3

138. Lessons learnt from multifaceted diagnostic approaches to the first 150 families in Victoria's Undiagnosed Diseases Program.

140. Analysis of the visual system in Friedreich ataxia

142. DEVELOPING NOVEL THERAPIES AND BIOMARKERS FOR FRIEDREICH ATAXIA: O14

146. Expanding the clinical and radiological phenotypes of leukoencephalopathy due to biallelic HMBS mutations

147. Evaluation of two population screening programmes for BRCA1/2 founder mutations in the Australian Jewish community: a protocol paper

148. Heterozygous ANKRD17 loss-of-function variants cause a syndrome with intellectual disability, speech delay, and dysmorphism

149. A step forward, but still inadequate: Australian health professionals’ views on the genetics and life insurance moratorium

150. Scoliosis in Friedreich's ataxia: longitudinal characterization in a large heterogeneous cohort

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