Phadke S - Search Results

1

Spectrum of Systemic Auto-Inflammatory Diseases in India: A Multi-Centric Experience.

Suri D, Rawat A, Jindal AK, Vignesh P, Gupta A, Pilania RK, Joshi V, Arora K, Kumrah R, Anjani G, Aggarwal A, Phadke S, Aboobacker FN, George B, Edison ES, Desai M, Taur P, Gowri V, Pandrowala AA, Bhattad S, Kanakia S, Gottorno M, Ceccherini I, Almeida de Jesus A, Goldbach-Mansky R, Hershfield MS, Singh S. Suri D, et al. Among authors: phadke s. Front Immunol. 2021 Mar 19;12:630691. doi: 10.3389/fimmu.2021.630691. eCollection 2021. Front Immunol. 2021. PMID: 33815380 Free PMC article.

2

Bowen-Conradi syndrome in an Indian infant: first non Hutterite case.

Gupta A, Phadke SR. Gupta A, et al. Among authors: phadke sr. Clin Dysmorphol. 2001 Apr;10(2):155-6. doi: 10.1097/00019605-200104000-00016. Clin Dysmorphol. 2001. PMID: 11310999

3

Novel NLRP12 variant presenting with familial cold autoimmunity syndrome phenotype.

Gupta L, Ahmed S, Singh B, Prakash S, Phadke S, Aggarwal A. Gupta L, et al. Among authors: phadke s. Ann Rheum Dis. 2021 Jul;80(7):e117. doi: 10.1136/annrheumdis-2019-216158. Epub 2019 Aug 24. Ann Rheum Dis. 2021. PMID: 31446425 No abstract available.

4

Clinical Sequencing Solves a Diagnostic Dilemma by Identifying a Novel Pathogenic Variant in USB1 Gene Causing Poikiloderma with Neutropenia.

Gangadharan H, Singh K, Phadke S, Aggarwal A. Gangadharan H, et al. Among authors: phadke s. Indian J Pediatr. 2021 Mar;88(3):270-271. doi: 10.1007/s12098-020-03502-w. Epub 2020 Sep 16. Indian J Pediatr. 2021. PMID: 32936385 No abstract available.

5

Monogenic Lupus with IgA Nephropathy Caused by Spondyloenchondrodysplasia with Immune Dysregulation.

Sait H, Gangadharan H, Gupta A, Aggarwal A, Jain M, Phadke SR. Sait H, et al. Indian J Pediatr. 2021 Aug;88(8):819-823. doi: 10.1007/s12098-020-03636-x. Epub 2021 Mar 13. Indian J Pediatr. 2021. PMID: 33712926

6

Does autopsy of antenatally diagnosed malformed foetuses aid genetic counselling?

Pahi J, Phadke SR, Halder A, Gupta A, Pandey R, Agarwal SS. Pahi J, et al. Among authors: phadke sr. Natl Med J India. 1998 Jul-Aug;11(4):169-70. Natl Med J India. 1998. PMID: 9808972

7

Malignant recessive osteopetrosis.

Phadke SR, Gupta A, Pahi J, Pandey A, Gautam P, Agarwal SS. Phadke SR, et al. Indian Pediatr. 1999 Jan;36(1):69-74. Indian Pediatr. 1999. PMID: 10709125 No abstract available.

8

Clinical profile of hereditary spherocytosis in North India.

Panigrahi I, Phadke SR, Agarwal A, Gambhir S, Agarwal SS. Panigrahi I, et al. Among authors: phadke sr. J Assoc Physicians India. 2002 Nov;50:1360-7. J Assoc Physicians India. 2002. PMID: 12583462

9

Spectrum of Lysosomal storage disorders at a medical genetics center in northern India.

Verma PK, Ranganath P, Dalal AB, Phadke SR. Verma PK, et al. Indian Pediatr. 2012 Oct;49(10):799-804. doi: 10.1007/s13312-012-0192-4. Epub 2012 Mar 30. Indian Pediatr. 2012. PMID: 22791670 Free article.

10

Aetiologic spectrum of mental retardation & developmental delay in India.

Aggarwal S, Bogula VR, Mandal K, Kumar R, Phadke SR. Aggarwal S, et al. Among authors: phadke sr. Indian J Med Res. 2012 Sep;136(3):436-44. Indian J Med Res. 2012. PMID: 23041737 Free PMC article.

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