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Keyword [tuberous sclerosis complex]
Result: 1 - 20 | Page: 1 of 4
1. The Clinical Study On Tuberous Sclerosis Complex And Mutational Analysis Of TSC2 In Cases Of A Pedigree
2. Study On Gene Mutation And MTOR Pathway Of Renal Vascular Smooth Muscle Lipoma Associated With Nodular Sclerosis
3. Screening And Functional Study Of Gene Mutations In Nodular Sclerosis And Pyogenic Sweatadenitis
4. (LAM) Gene Mutation Screening And Plasma Free DNA Detection And Nodular Sclerosis (TSC) Lung Performance Summary And Analysis
5. The Involvement Of SVZ-derived Neural Precursor Cells In The Epileptogenicity Of Malformations Of Cortical Development
6. The Role Of TSC1and TSC2Tumor Suppressors In ER Stress Response
7. The Roles And Mechanisms Of Nogo-A In Malformations Of Cortical Development
8. The Role Of Matrix Metalloproteinase9in Malformations Of Cortical Development
9. Identification Of Novel TSC2 Mutations In Patients With Tuberous Sclerosis Complex
10. Mutation Analysis Of TSC1 And TSC2 Genes In Three Chinese Patients With Tuberous Sclerosis Complex
11. Analysis Of Gene Mutations In Two Chinese Patients With Tuberous Sclerosis Complex
12. Clinical Analysis Of 14 Tuberous Sclerosis Complex Cases With Pulmonary Involvement
13. Gene Mutation Analysis Of Duchenne Muscular Dystrophy And Tuberous Sclerosis Complex
14. Efficacy Of Combined Inhibition Of MTOR And ERK/MAPK Signaling Pathways In Treating A Tuberous Sclerosis Complex Cell Model
15. Gene Mutation Of FSHR And LHCGR In The Patients With Hypergonadotrophic Amenorrhea Or Poor Ovarian Reaction And Mutation Screening And Prenatal Diagnosis In 14 Families With Tuberous Sclerosis Complex
16. Molecular Genetic Analysis Of A Chinese Family With Tuberous Sclerosis Complex
17. Mutation Analysis Of TSC1 And TSC2 Genes In Chinese Patients With Tuberous Sclerosis
18. Mutation Analysis Of Tsc1 And Tsc2 Genes In Chinese Patients With Tuberous Sclerosis
19. The Relation Between Brain MRI Lesion Load And Epilepsy Secondary To Tuberous Sclerosis Complex
20. The Role Of IL-17in Epilepsy With Malformations Of Cortical Development
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