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

Year Number of Results
1874 3
1876 4
1879 3
1880 2
1881 7
1882 6
1884 3
1885 3
1886 1
1887 1
1888 8
1889 3
1890 2
1891 7
1892 6
1893 1
1903 1
1905 1
1925 1
1927 1
1928 2
1930 1
1931 1
1933 1
1935 2
1939 2
1940 1
1941 2
1942 3
1943 3
1944 2
1945 13
1946 8
1947 6
1948 2
1949 8
1950 5
1951 4
1952 5
1954 4
1955 9
1956 7
1957 11
1958 17
1959 15
1960 17
1961 26
1962 42
1963 53
1964 48
1965 71
1966 69
1967 79
1968 82
1969 96
1970 96
1971 118
1972 149
1973 172
1974 121
1975 122
1976 151
1977 160
1978 182
1979 207
1980 205
1981 194
1982 197
1983 261
1984 266
1985 229
1986 269
1987 272
1988 267
1989 304
1990 339
1991 369
1992 394
1993 387
1994 420
1995 431
1996 477
1997 518
1998 539
1999 605
2000 1055
2001 682
2002 763
2003 899
2004 1058
2005 1255
2006 1346
2007 1514
2008 1830
2009 2163
2010 2549
2011 2900
2012 3400
2013 3775
2014 4011
2015 4488
2016 4725
2017 4898
2018 5335
2019 5914
2020 7399
2021 8822
2022 9226
2023 9008
2024 9371
2025 9558
2026 51

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104,177 results

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Page 1
Shah-Waardenburg syndrome.
Mahmoudi A, Rami M, Khattala K, Elmadi A, Afifi MA, Youssef B. Mahmoudi A, et al. Pan Afr Med J. 2013;14:60. doi: 10.11604/pamj.2013.14.60.1543. Epub 2013 Feb 12. Pan Afr Med J. 2013. PMID: 23565307 Free PMC article.
Shah-Waardenburg syndrome (SWS) is a neurocristopathy and is characterized by Hirschsprung's disease (HD), deafness, and depigmentation of hairs, skin, and iris. ...
Shah-Waardenburg syndrome (SWS) is a neurocristopathy and is characterized by Hirschsprung's disease (HD), deafness, and depigmentati …
Case of Waardenburg Shah syndrome in a family with review of literature.
Chandra Mohan SLN. Chandra Mohan SLN. J Otol. 2018 Sep;13(3):105-110. doi: 10.1016/j.joto.2018.05.005. Epub 2018 Jun 8. J Otol. 2018. PMID: 30559775 Free PMC article. Review.
Waardenburg syndrome type 4, also called as Waardenburg Shah Syndrome is a very rare congenital disorder with astounding variable clinical expression, characterized by pigmentary abnormalities of the hair (A white forelock of hair, premature graying) and pigmentary changes …
Waardenburg syndrome type 4, also called as Waardenburg Shah Syndrome is a very rare congenital disorder with astounding variable cli …
Dr. Raksha M Shah: A living legend.
Shah V. Shah V. J Oral Maxillofac Pathol. 2023 Jan-Mar;27(1):2-3. doi: 10.4103/jomfp.jomfp_88_23. Epub 2023 Mar 21. J Oral Maxillofac Pathol. 2023. PMID: 37234307 Free PMC article. No abstract available.
Waardenburg-Shah syndrome rare and challenging case report from Somalia.
Abdi AM, Ali AY, Göl IH. Abdi AM, et al. Int J Surg Case Rep. 2022 Apr;93:106952. doi: 10.1016/j.ijscr.2022.106952. Epub 2022 Mar 15. Int J Surg Case Rep. 2022. PMID: 35313185 Free PMC article.
INTRODUCTION AND IMPORTANCE: Waardenburg-Shah disorder could be an uncommon autosomal recessive inherited ailment characterized by aganglionic megacolon with a high mortality rate. ...Here we present a case with typical presentation of Waardenburg Shah syndrome. CAS …
INTRODUCTION AND IMPORTANCE: Waardenburg-Shah disorder could be an uncommon autosomal recessive inherited ailment characterized by ag …
The Shah's spleen.
Cervantes J, Baley I. Cervantes J, et al. J Am Coll Surg. 2011 Aug;213(2):340; author reply 340-1. doi: 10.1016/j.jamcollsurg.2011.04.010. J Am Coll Surg. 2011. PMID: 21787996 No abstract available.
Meaning.
Shah S. Shah S. Pediatr Crit Care Med. 2024 Jun 1;25(6):561-562. doi: 10.1097/PCC.0000000000003481. Epub 2024 Feb 26. Pediatr Crit Care Med. 2024. PMID: 40315042 No abstract available.
When millimeters matter.
Shah BR. Shah BR. Eur Radiol. 2024 Aug;34(8):5164-5166. doi: 10.1007/s00330-024-10757-w. Epub 2024 Jun 10. Eur Radiol. 2024. PMID: 38856783 No abstract available.
Editorial Commentary.
Shah O. Shah O. Urol Pract. 2022 Nov;9(6):573. doi: 10.1097/UPJ.0000000000000347.01. Epub 2022 Sep 21. Urol Pract. 2022. PMID: 37145825 No abstract available.
104,177 results
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