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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1992 1
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1998 1
2006 2
2012 1
2024 0

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Page 1
Gradenigo's syndrome.
Rangasami JJ, Puliyel J. Rangasami JJ, et al. Indian Pediatr. 2006 May;43(5):456-7. Indian Pediatr. 2006. PMID: 16735775 Free article. No abstract available.
Loss-of-function mutations in IGSF1 cause an X-linked syndrome of central hypothyroidism and testicular enlargement.
Sun Y, Bak B, Schoenmakers N, van Trotsenburg AS, Oostdijk W, Voshol P, Cambridge E, White JK, le Tissier P, Gharavy SN, Martinez-Barbera JP, Stokvis-Brantsma WH, Vulsma T, Kempers MJ, Persani L, Campi I, Bonomi M, Beck-Peccoz P, Zhu H, Davis TM, Hokken-Koelega AC, Del Blanco DG, Rangasami JJ, Ruivenkamp CA, Laros JF, Kriek M, Kant SG, Bosch CA, Biermasz NR, Appelman-Dijkstra NM, Corssmit EP, Hovens GC, Pereira AM, den Dunnen JT, Wade MG, Breuning MH, Hennekam RC, Chatterjee K, Dattani MT, Wit JM, Bernard DJ. Sun Y, et al. Among authors: rangasami jj. Nat Genet. 2012 Dec;44(12):1375-81. doi: 10.1038/ng.2453. Epub 2012 Nov 11. Nat Genet. 2012. PMID: 23143598 Free PMC article.
Asian MODY: are we missing an important diagnosis?
Porter JR, Rangasami JJ, Ellard S, Gloyn AL, Shields BM, Edwards J, Anderson JM, Shaw NJ, Hattersley AT, Frayling TM, Plunkett M, Barrett TG. Porter JR, et al. Among authors: rangasami jj. Diabet Med. 2006 Nov;23(11):1257-60. doi: 10.1111/j.1464-5491.2006.01958.x. Diabet Med. 2006. PMID: 17054605
Familial precocious puberty in girls.
Rangasami JJ, Grant DB. Rangasami JJ, et al. J R Soc Med. 1992 Aug;85(8):497-8. doi: 10.1177/014107689208500826. J R Soc Med. 1992. PMID: 1404207 Free PMC article. No abstract available.