26 results on '"Soltanzadeh, Payam"'
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2. Myopathies
3. Myofibrillar myopathy presenting with an inclusion body myositis‐like phenotype
4. Zilucoplan in immune-mediated necrotising myopathy: a phase 2, randomised, double-blind, placebo-controlled, multicentre trial
5. Using Intensity Modulated Radiation Therapy for the Treatment of Sialorrhea in Amyotrophic Lateral Sclerosis
6. Study Design of AOC 1001-CS1, a Phase 1/2 Clinical Trial Evaluating the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of AOC 1001 Administered Intravenously to Adult Patients with Myotonic Dystrophy Type 1 (DM1) (MARINA) (S23.006)
7. Myotonic Dystrophies: A Genetic Overview
8. Clinical and genetic characterization of manifesting carriers of DMD mutations
9. Nonsense mutation-associated Becker muscular dystrophy: interplay between exon definition and splicing regulatory elements within the DMD gene
10. In silico and in vitro effects of the I30T mutation on myelin protein zero instability in the cell membrane
11. Mutational Spectrum of DMD Mutations in Dystrophinopathy Patients: Application of Modern Diagnostic Techniques to a Large Cohort
12. Giant congenital melanocytic nevus with neurofibroma-like changes and spina bifida occulta
13. In silico and in vitro effects of the I30T mutation on myelin protein zero instability in the cell membrane.
14. Phenotypic Heterogeneity in Limb-girdle Muscular Dystrophy Type 2L (Anoctaminopathy) (P5.446)
15. Rapidly Progressive POEMS Syndrome with Absent M protein in Serum or Urine, Normal Bone Survey, and Normal Non-targeted Bone Marrow Biopsy (P2.448)
16. Anti-3-hydroxy-3-methylglutaryl-coenzyme a reductase autoantibody-positive necrotizing autoimmune myopathy with dermatomyositis-like eruption
17. Diagnostic challenges in POEMS syndrome presenting with polyneuropathy: A case series
18. Intravascular T cell Lymphoma: A Rare, Poorly Characterized Entity with Cytotoxic Phenotype (P4.060)
19. Correction: A Mutation Causes MuSK Reduced Sensitivity to Agrin and Congenital Myasthenia
20. Kikuchi's Disease: An Unrecognized Cause of Aseptic Meningitis (P06.215)
21. A Mutation Causes MuSK Reduced Sensitivity to Agrin and Congenital Myasthenia
22. Wilson’s Disease: A Great Masquerader
23. A Mutation Causes MuSK Reduced Sensitivity to Agrin and Congenital Myasthenia.
24. Wilson’s Disease: A Great Masquerader.
25. Heterogeneous Presentations and Serologies in Myasthenia Gravis Patients Presenting with Dysphagia.
26. Using Intensity Modulated Radiation Therapy for the Treatment of Sialorrhea in Amyotrophic Lateral Sclerosis.
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