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

Year Number of Results
1857 1
1872 1
1878 1
1883 1
1885 2
1886 1
1887 1
1888 1
1947 2
1948 3
1949 1
1950 18
1951 11
1952 5
1953 5
1954 8
1955 14
1956 19
1957 8
1958 10
1959 11
1960 13
1961 12
1962 7
1963 6
1964 9
1965 13
1966 11
1967 10
1968 16
1969 15
1970 2
1971 4
1972 5
1973 12
1974 7
1975 7
1976 5
1977 10
1978 7
1979 13
1980 9
1981 18
1982 14
1983 23
1984 26
1985 28
1986 38
1987 34
1988 36
1989 26
1990 37
1991 34
1992 41
1993 28
1994 48
1995 54
1996 62
1997 69
1998 57
1999 68
2000 103
2001 85
2002 91
2003 104
2004 120
2005 135
2006 161
2007 136
2008 160
2009 204
2010 193
2011 237
2012 259
2013 242
2014 275
2015 267
2016 286
2017 309
2018 358
2019 358
2020 349
2021 408
2022 370
2023 338
2024 326
2025 252

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6,451 results

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Page 1
Clinical details of individuals with Rauch-Steindl syndrome due to NSD2 truncating variants.
Nishi E, Yanagi K, Kaname T, Okamoto N. Nishi E, et al. Mol Genet Genomic Med. 2024 Feb;12(2):e2396. doi: 10.1002/mgg3.2396. Mol Genet Genomic Med. 2024. PMID: 38353053 Free PMC article.
BACKGROUND: Rauch-Steindl syndrome (RAUST) is a very rare genetic syndrome caused by a pathogenic variant in NSD2 on chromosome 4p16.3. ...
BACKGROUND: Rauch-Steindl syndrome (RAUST) is a very rare genetic syndrome caused by a pathogenic variant in NSD2 on chromosome 4p16. …
Foreword.
Rauch TM. Rauch TM. Mil Med. 2023 Nov 8;188(Supplement_6):1. doi: 10.1093/milmed/usad190. Mil Med. 2023. PMID: 37948267 No abstract available.
[Winter sports injuries].
Rauch A, Martetschläger F. Rauch A, et al. Orthopadie (Heidelb). 2022 Nov;51(11):868-869. doi: 10.1007/s00132-022-04320-y. Epub 2022 Nov 14. Orthopadie (Heidelb). 2022. PMID: 36376758 Free PMC article. German. No abstract available.
Medical Appointment-Prof. Rauch.
[No authors listed] [No authors listed] Iowa Med J. 1857 Aug;4(2):155-156. Iowa Med J. 1857. PMID: 37677621 Free PMC article. No abstract available.
Severe manifestation of Rauch-Azzarello syndrome associated with biallelic deletion of CTNND2.
Pauly M, Krumbiegel M, Trumpp S, Braig S, Rupprecht T, Kraus C, Uebe S, Reis A, Vasileiou G. Pauly M, et al. Clin Genet. 2024 Aug;106(2):180-186. doi: 10.1111/cge.14532. Epub 2024 Apr 11. Clin Genet. 2024. PMID: 38604781
To date, only heterozygous loss-of-function CTNND2 variants have been associated with mild neurodevelopmental delay and behavioral anomalies, a condition, which we named Rauch-Azzarello syndrome. Here, we report three siblings of a consanguineous family of Syrian descent w …
To date, only heterozygous loss-of-function CTNND2 variants have been associated with mild neurodevelopmental delay and behavioral anomalies …
Joseph Rauch.
Dunning RE. Dunning RE. S Afr Med J. 1974 Oct 26;48(52):2198. S Afr Med J. 1974. PMID: 4610812 No abstract available.
Forward.
Rauch TM. Rauch TM. Mil Med. 2019 Mar 1;184(Suppl 1):1. doi: 10.1093/milmed/usy354. Mil Med. 2019. PMID: 30901462 No abstract available.
Forward.
Rauch TM. Rauch TM. Mil Med. 2021 Jan 25;186(Suppl 1):5. doi: 10.1093/milmed/usaa430. Mil Med. 2021. PMID: 33499540 No abstract available.
Foreword.
Rauch TM. Rauch TM. Mil Med. 2025 Sep 1;190(Supplement_2):1. doi: 10.1093/milmed/usaf240. Mil Med. 2025. PMID: 40984071 No abstract available.
Forward.
Rauch TM. Rauch TM. Mil Med. 2018 Mar 1;183(suppl_1):1. doi: 10.1093/milmed/usx190. Mil Med. 2018. PMID: 29635593 No abstract available.
6,451 results