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1. HostSeq: a Canadian whole genome sequencing and clinical data resource

3. P76 The Canadian neuromuscular disease registry: a national spinal muscular atrophy registry for real world evidence

4. Additional file 1 of HostSeq: a Canadian whole genome sequencing and clinical data resource

6. HostSeq : A Canadian Whole Genome Sequencing and Clinical Data Resource

7. MOTOR NEURON DISORDERS AND NEUROPATHIES

8. REGISTRIES AND CARE OF NMD

10. Development of a standard of care for patients with valosin-containing protein associated multisystem proteinopathy

17. The Canadian Neuromuscular Disease Registry 2010–2019: A Decade of Facilitating Clinical Research Througha Nationwide, Pan-NeuromuscularDisease Registry

24. Analysis of emotions in text-based negotiations

37. A.P.2

38. P32 Mutations in SPG7 cause chronic progressive external ophthalmoplegia through disordered mtDNA maintenance

40. The Gadaba and the 'non-ST' Desia of Koraput, Orissa

42. New treatments for mitochondrial disease-no time to drop our standards.

45. P.15.7 A founder mutation in the titin gene is a common cause of myofibrillar myopathy with early respiratory failure

46. O.4 Proteomic analysis confirms that HMERF associated with mutations in A-band titin is a new subtype of myofibrillar myopathies

47. Titin founder mutation is a common cause of myofibrillar myopathy with early respiratory failure

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