20 results on '"Sud R"'
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2. Bridging the equity gap in patient education: the biliary tract cancer BABEL project
3. Non-synaptic mechanisms of antipsychotics may be key to their actions
4. P.293 - Classic congenital myopathy with recessive mutations in genes encoding ion channels: clinical phenotype and good response to acetazolamide
5. P.229 - Skeletal muscle channelopathies: Rare treatable disorders with common presentation in childhood
6. P.230 - Large scale validation of functional expression of ClC-1 variants in genetic counselling of myotonia congenital
7. NMJ+C05 - Improving genetic diagnosis and counselling for patients with myotoniacongenita
8. NMJ+C07 - Diagnosing the undiagnosable: a targeted approach to genetic sequencingin unconfi rmed cases of skeletal muscle channelopathies
9. NMJ+C02 - Hypokalaemic periodic paralysis due to a novel ATP1A2 mutation: a new periodic paralysis gene?
10. Vie, travail et santé des salariés de la sous-traitance du nucléaire
11. Vie, travail et santé des salariés de la sous-traitance du nucléaire
12. G.P.101 New immunohistochemical method for improved myotonia and chloride channel mutation diagnostics
13. Vie, travail et santé des salariés de la sous-traitance du nucléaire
14. P39 Prevalence study of skeletal muscle channelopathies in England
15. P30 Large scale chloride channel gene DNA rearrangements are an important cause of recessive myotonia congenitaimplications for diagnostic screening
16. P24 Genetic heterogeneity and mechanisms of phenotypic variability in human skeletal muscle channelopathies – a new S4 mutation not associated with HypoPP
17. P91 Using MRI as a diagnostic tool in the skeletal muscle channelopathies
18. P43 Acetazolamide response in patients affected by hypokalemic periodic paralysis
19. Transcriptosome Profiling of B-CLL Identifies WNT-3A and ROR-1 as an Autocrine Mechanism in Cell Survival.
20. FOLLOW-UP OF SURVIVORS OF EPIDEMIC VENO-OCCLUSIVE DISEASE IN INDIA
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