29 results on '"CAMELO, Clara Gontijo"'
Search Results
2. Cross-sectional survey study of the natural history of LAMA2-related dystrophy
3. Hypoglycemia in Patients With LAMA2-CMD
4. Genetic profile of Brazilian patients with LAMA2‐related dystrophies
5. Clinical features of collagen VI-related dystrophies: A large Brazilian cohort
6. European Joint Programme on Rare Diseases workshop: LAMA2-muscular dystrophy: paving the road to therapy March 17–19, 2023, Barcelona, Spain
7. Marked neuropsychiatric involvement and dysmorphic features in nemaline myopathy
8. Child Neurology: A case of FHL1-related disease presenting as inflammatory myopathy
9. Central nervous system involvement and the genotype-phenotype correlation in CMD-LAMA2
10. Hypoglycemia in patients with LAMA2-CMD
11. Muscle ultrasound as a tool for respiratory assessment in patients with LAMA2-MD
12. Brain MRI Abnormalities, Epilepsy and Intellectual Disability in LAMA2 Related Dystrophy – a Genotype/Phenotype Correlation
13. Clinical Manifestation of Nebulin-Associated Nemaline Myopathy
14. Effect of the COVID-19 pandemic on patients with inherited neuromuscular disorders
15. The Location of Disease-Causing DES Variants Determines the Severity of Phenotype and the Morphology of Sarcoplasmic Aggregates
16. Effect of the COVID-19 pandemic on patients with inherited neuromuscular disorders
17. European Joint Programme on Rare Diseases workshop: LAMA2-muscular dystrophy: paving the road to therapy March 17–19, 2023, Barcelona, Spain
18. Location of Disease-Causing DES Variants Determines the Severity of Phenotype and the Morphology of Sarcoplasmic Aggregates.
19. Severe progressive brain involvement in a patient with TRMT10C mutation
20. Child Neurology: A Case of FHL1-Related Disease Presenting as Inflammatory Myopathy
21. Facial myokymia in inherited peripheral nerve hyperexcitability syndrome
22. The Location of Disease-Causing DESVariants Determines the Severity of Phenotype and the Morphology of Sarcoplasmic Aggregates
23. Unilateral abdominal protrusion as the main diagnostic sign of facioscapulohumeral dystrophy
24. Unilateral abdominal protrusion as the main diagnostic sign of facioscapulohumeral dystrophy
25. Child Neurology: A Case of -Related Disease Presenting as Inflammatory Myopathy.
26. A DOENÇA HEPÁTICA GORDUROSA NÃO-ALCOÓLICA: UM ESTUDO DE COORTE COM FOCO NA RESPOSTA AO TRATAMENTO COM ORIENTAÇÃO NUTRICIONAL
27. Nonalcoholic fatty liver disease: a cohort study focusing on treatment response to nutritional counseling
28. Nonalcoholic fatty liver disease: a cohort study focusing on treatment response to nutritional counseling
29. Child Neurology: A Case of FHL1 -Related Disease Presenting as Inflammatory Myopathy.
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