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3. Genetic variant profiling of neonatal diabetes mellitus in Iranian patients: Unveiling 58 distinct variants in 14 genes.

12. Association of AHSG with alopecia and mental retardation (APMR) syndrome

14. Association of SOD2 rs2758339, rs5746136 and rs2842980 polymorphisms with increased risk of breast cancer: a haplotype-based case–control study.

16. Influence of social indices on demand and supply policies in petrol stations with congested queue

17. Causative variants linked with limb girdle muscular dystrophy in an Iranian population: 6 novel variants.

18. Mutations in GMPPB cause congenital myasthenic syndrome and bridge myasthenic disorders with dystroglycanopathies

19. Experiences of caring cancer patients at home: The experiences of the healthcare professionals. : A qualitative literature review

20. Genetic Analysis of MECP2 Gene in Iranian Patients with Rett Syndrome

21. An ancestral 10-bp repeat expansion in VWA1 causes recessive hereditary motor neuropathy

22. Upplevelser av att vårda cancerpatienter palliativt i hemmet: Sjukvårdspersonalens upplevelser. : En kvalitativ litteraturstudie

23. Infantile Neuroaxonal Dystrophy in Two Cases: Siblings with Different Presentations.

25. Therapeutic Effects of Adrenocorticotropic Hormone ACTH in Children with Severely Intractable Seizure

26. The Role of Emotional processing in Predicting Adaptability in Female Students Diagnosed with Oppositional Defiant Disorder

28. Recessive Charcot-Marie-Tooth and multiple sclerosis associated with a variant in MCM3AP

29. Motor neuron diseases caused by a novel VRK1 variant - A genotype/phenotype study

30. An ancestral 10-bp repeat expansion in VWA1 causes recessive hereditary motor neuropathy.

34. Clinical features of the myasthenic syndrome arising from mutations in GMPPB

35. A novel mutation in the aprataxin (APTX) gene in an Iranian individual suffering early-onset ataxia with oculomotor apraxia type 1(AOA1) disease

41. Mutations inGMPPBcause congenital myasthenic syndrome and bridge myasthenic disorders with dystroglycanopathies

47. A novel homozygous DPH1mutation causes intellectual disability and unique craniofacial features

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