Shah H - Search Results

1

Clinical and mutation profile of multicentric osteolysis nodulosis and arthropathy.

Bhavani GS, Shah H, Shukla A, Gupta N, Gowrishankar K, Rao AP, Kabra M, Agarwal M, Ranganath P, Ekbote AV, Phadke SR, Kamath A, Dalal A, Girisha KM. Bhavani GS, et al. Among authors: shah h. Am J Med Genet A. 2016 Feb;170A(2):410-417. doi: 10.1002/ajmg.a.37447. Epub 2015 Nov 24. Am J Med Genet A. 2016. PMID: 26601801

2

Second report of slipped capital femoral epiphysis in Rubinstein-Taybi syndrome.

Shah H, Singh G, Vijayan S, Girisha KM. Shah H, et al. Clin Dysmorphol. 2011 Jan;20(1):55-57. doi: 10.1097/MCD.0b013e32833f000b. Clin Dysmorphol. 2011. PMID: 20808218 No abstract available.

3

Hypoplasia/aplasia of pelvis, femora, fibulae, ulna, digits and nails: Fuhrmann syndrome without WNT7A mutations.

Girisha KM, Vasudevan TG, Saadi AV, Shah H, Gopinath PM, Satyamoorthy K. Girisha KM, et al. Among authors: shah h. Clin Dysmorphol. 2011 Oct;20(4):205-209. doi: 10.1097/MCD.0b013e328348d956. Clin Dysmorphol. 2011. PMID: 21716096 No abstract available.

4

Environmental tobacco and wood smoke increase the risk of Legg-Calvé-Perthes disease.

Daniel AB, Shah H, Kamath A, Guddettu V, Joseph B. Daniel AB, et al. Among authors: shah h. Clin Orthop Relat Res. 2012 Sep;470(9):2369-75. doi: 10.1007/s11999-011-2180-8. Clin Orthop Relat Res. 2012. PMID: 22090357 Free PMC article.

5

Further characterization of acro-renal-uterine-mandibular syndrome: report of a case and review of earlier reports.

Girisha KM, Pratap D, Shah HH. Girisha KM, et al. Among authors: shah hh. Clin Dysmorphol. 2012 Apr;21(2):83-86. doi: 10.1097/MCD.0b013e328350ae74. Clin Dysmorphol. 2012. PMID: 22391619 Review. No abstract available.

6

Handedness in diplegic cerebral palsy.

Lin KR, Prabhu V, Shah H, Kamath A, Joseph B. Lin KR, et al. Among authors: shah h. Dev Neurorehabil. 2012;15(5):386-9. doi: 10.3109/17518423.2012.696736. Epub 2012 Jul 3. Dev Neurorehabil. 2012. PMID: 22758776

7

Growth retardation, intellectual disability, facial anomalies, cataract, thoracic hypoplasia, and skeletal abnormalities: a novel phenotype.

Shah H, Bens S, Caliebe A, Graham JM Jr, Girisha KM. Shah H, et al. Am J Med Genet A. 2012 Nov;158A(11):2941-5. doi: 10.1002/ajmg.a.35618. Epub 2012 Sep 17. Am J Med Genet A. 2012. PMID: 22987502 Free PMC article.

8

Analysis of the WISP3 gene in Indian families with progressive pseudorheumatoid dysplasia.

Dalal A, Bhavani G SL, Togarrati PP, Bierhals T, Nandineni MR, Danda S, Danda D, Shah H, Vijayan S, Gowrishankar K, Phadke SR, Bidchol AM, Rao AP, Nampoothiri S, Kutsche K, Girisha KM. Dalal A, et al. Among authors: shah h. Am J Med Genet A. 2012 Nov;158A(11):2820-8. doi: 10.1002/ajmg.a.35620. Epub 2012 Sep 17. Am J Med Genet A. 2012. PMID: 22987568

9

Loss of a condyle of the femur or tibia following septic arthritis in infancy: problems of management and testing of a hypothesis of pathogenesis.

Tercier S, Siddesh ND, Shah H, Girisha KM, Joseph B. Tercier S, et al. Among authors: shah h. J Child Orthop. 2012 Aug;6(4):319-25. doi: 10.1007/s11832-012-0408-0. Epub 2012 Jul 19. J Child Orthop. 2012. PMID: 23904899 Free PMC article.

10

A syndrome of facial dysmorphism, cubital pterygium, short distal phalanges, swan neck deformity of fingers, and scoliosis.

Girisha KM, Abdollahpour H, Shah H, Bhavani GS, Graham JM Jr, Boggula VR, Phadke SR, Kutsche K. Girisha KM, et al. Among authors: shah h. Am J Med Genet A. 2014 Apr;164A(4):1035-40. doi: 10.1002/ajmg.a.36381. Epub 2014 Jan 23. Am J Med Genet A. 2014. PMID: 24458843

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