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Publications by T P Melo
Autosomal Dominant Cerebellar Ataxia With Deafness, Myoclonus and Amyotrophy.
Journal of Neurology, Neurosurgery and Psychiatry
Psychiatry
Mental Health
Neurology
Surgery
Related publications
Myoclonus-Cerebellar Ataxia-Deafness Syndrome
A Case of 16q Linked Autosomal Dominant Cerebellar Ataxia (16q-Adca) Presenting Dystonia
Clinical Neurology
Neurology
Adult-Onset Autosomal Recessive Cerebellar Ataxia
Infantile-Onset Autosomal Recessive Nonprogressive Cerebellar Ataxia
Autosomal Recessive Cerebellar Ataxia Due to STUB1 Deficiency
Autosomal Dominant Familial Hypoparathyroidism and Sensorineural Deafness Without Renal Dysplasia
European Journal of Endocrinology
Medicine
Endocrinology
Metabolism
Diabetes
Autosomal Recessive Congenital Cerebellar Ataxia Due to MGLUR1 Deficiency
A Linkage Disequilibrium at the Candidate Gene Locus for 16q-Linked Autosomal Dominant Cerebellar Ataxia Type III in Japan
Journal of Human Genetics
Genetics
Meningococcal Meningitis Presenting With Bilateral Deafness and Ataxia.
Postgraduate Medical Journal
Medicine
