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101. 15 years of research on Oral-Facial-Digital syndromes: from 1 to 16 causal genes

102. Management of Severe Developmental Regression in an Autistic Child with a 1q21.3 Microdeletion and Self-Injurious Blindness

103. Cognitive impairment in children with CACNA1A mutations.

104. Expanding the genetic and phenotypic relevance of KCNB1 variants in developmental and epileptic encephalopathies: 27 new patients and overview of the literature.

105. Reverse-Transcriptase Inhibitors in the Aicardi–Goutières Syndrome

106. A decision tree for the genetic diagnosis of deficiency of adenosine deaminase 2 (DADA2): a French reference centres experience

107. Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders

108. Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders

109. Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU

110. Exhaustive analysis of BH4 and dopamine biosynthesis genes in patients with Dopa-responsive dystonia

114. TBC1D24 genotype-phenotype correlation

117. Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders

118. Additional file 1: of Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhoodâ a study of 155 patients

119. Additional file 5: of Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhoodâ a study of 155 patients

120. Additional file 2: of Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhoodâ a study of 155 patients

121. Additional file 4: of Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhoodâ a study of 155 patients

122. Additional file 3: of Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhoodâ a study of 155 patients

123. Biallelic PDE2Avariants: a new cause of syndromic paroxysmal dyskinesia

124. Expanding the phenotypic spectrum of Allan-Herndon-Dudley syndrome in patients with SLC16A2 mutations.

126. TMEM107 recruits ciliopathy proteins to subdomains of the ciliary transition zone and causes Joubert syndrome

127. TMEM107 recruits ciliopathy proteins to subdomains of the ciliary transition zone and causes Joubert syndrome

128. Cognitive disorders in patients with CACNA1A mutations

130. ARID1Bmutations are the major genetic cause of corpus callosum anomalies in patients with intellectual disability

131. TBC1D24genotype–phenotype correlation

134. Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood-a study of 155 patients.

135. Benign paroxysmal torticollis, benign paroxysmal vertigo, and benign tonic upward gaze are not benign disorders.

136. De novo variants in FBXO11cause a syndromic form of intellectual disability with behavioral problems and dysmorphisms

137. Etude clinique et génétique chez 80 patients atteints de syndrome de Joubert

138. TMEM107 recruits ciliopathy proteins to subdomains of the ciliary transition zone and causes Joubert syndrome

139. ADCY5-related dyskinesia

140. A recurrent KCNQ2 pore mutation causing early onset epileptic encephalopathy has a moderate effect on M current but alters subcellular localization of Kv7 channels

141. Hypomorphic variants of cationic amino acid transporter 3 in males with autism spectrum disorders

143. Xp21 deletion in female patients with intellectual disability: Two new cases and a review of the literature

144. Biallelic mutations in the homeodomain of NKX6-2 underlie a severe hypomyelinating leukodystrophy.

145. Fifteen years of research on oral-facial-digital syndromes: from 1 to 16 causal genes.

146. Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU.

147. Homozygous MTTP and APOB mutations may lead to hepatic steatosis and fibrosis despite metabolic differences in congenital hypocholesterolemia

149. NovelKCNQ2andKCNQ3Mutations in a Large Cohort of Families with Benign Neonatal Epilepsy: First Evidence for an Altered Channel Regulation by Syntaxin-1A

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