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101. List of contributors

102. Clinical sites of the Undiagnosed Diseases Network: unique contributions to genomic medicine and science

106. De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia

112. Erratum. TFAM Enhances Fat Oxidation and Attenuates High-Fat Diet–Induced Insulin Resistance in Skeletal Muscle. Diabetes 2019;68:1552–1564

114. Molecular Transducers of Physical Activity Consortium (MoTrPAC): Mapping the Dynamic Responses to Exercise

116. De novo EIF2AK1 and EIF2AK2 Variants Are Associated with Developmental Delay, Leukoencephalopathy, and Neurologic Decompensation

118. Partial Loss of USP9X Function Leads to a Male Neurodevelopmental and Behavioral Disorder Converging on Transforming Growth Factor β Signaling

120. Impaired Muscle Mitochondrial Function in Familial Partial Lipodystrophy.

125. Mitochondrial respiratory states and rates

131. Magnetic Resonance Imaging characteristics in case of TOR1AIP1 muscular dystrophy

132. De Novo Pathogenic Variants in N-cadherin Cause a Syndromic Neurodevelopmental Disorder with Corpus Callosum, Axon, Cardiac, Ocular, and Genital Defects

134. De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia

137. Lysosomal Storage and Albinism Due to Effects of a De Novo CLCN7 Variant on Lysosomal Acidification

138. TFAM Enhances Fat Oxidation and Attenuates High-Fat Diet–Induced Insulin Resistance in Skeletal Muscle

142. Correction: Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations

143. Variants in PRKAR1Bcause a neurodevelopmental disorder with autism spectrum disorder, apraxia, and insensitivity to pain

144. Commonalities across computational workflows for uncovering explanatory variants in undiagnosed cases

145. Distinct Influence of Omega-3 Fatty Acids on the Plasma Metabolome of Healthy Older Adults.

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