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102. Longitudinal Synaptic Loss in Primary Tauopathies: An In Vivo [11 C] UCB‐J Positron Emission Tomography Study

103. Age‐related telomere attrition in the human putamen

107. The clinical syndrome of dystonia with anarthria/aphonia

109. Biallelic variants in TSPOAP1, encoding the active-zone protein RIMBP1, cause autosomal recessive dystonia

111. Functional movement disorder gender, age and phenotype study

114. Stridor in multiple system atrophy: Consensus statement on diagnosis, prognosis, and treatment

116. Functional connectivity moderates the impact of synaptic loss on behaviour in frontotemporal lobar degeneration syndromes.

117. Clinical aspects of endocrinology: parathyroid and adrenal cortex disorders.

118. Isolated Cervical Dystonia: Diagnosis and Classification

120. A Screening Tool to Quickly Identify Movement Disorders in Patients with Inborn Errors of Metabolism

124. Critical care admission following elective surgery was not associated with survival benefit: prospective analysis of data from 27 countries

125. No genetic association between attention-deficit/hyperactivity disorder (ADHD) and Parkinson’s disease in nine ADHD candidate SNPs

126. Current Opinions and Areas of Consensus on the Role of the Cerebellum in Dystonia

128. Detection and Characterization of a De Novo Alu Retrotransposition Event Causing NKX2‐1‐Related Disorder

133. Pallidal neurostimulation in patients with medication-refractory cervical dystonia: a randomised, sham-controlled trial

142. Treatable inherited rare movement disorders

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