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

Year Number of Results
1856 1
1927 1
1930 1
1946 1
1947 2
1948 1
1949 5
1950 5
1951 3
1952 2
1953 2
1954 2
1955 3
1956 2
1957 6
1958 4
1959 9
1960 1
1961 3
1962 3
1963 6
1964 6
1965 7
1966 7
1967 13
1968 6
1969 15
1970 9
1971 10
1972 3
1973 8
1974 10
1975 5
1976 10
1977 10
1978 11
1979 17
1980 17
1981 15
1982 22
1983 23
1984 13
1985 26
1986 17
1987 20
1988 24
1989 23
1990 15
1991 16
1992 27
1993 24
1994 27
1995 26
1996 29
1997 46
1998 35
1999 27
2000 46
2001 46
2002 24
2003 35
2004 31
2005 48
2006 59
2007 40
2008 50
2009 55
2010 56
2011 50
2012 56
2013 64
2014 58
2015 69
2016 59
2017 53
2018 56
2019 66
2020 93
2021 103
2022 73
2023 63
2024 85
2025 37

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1,978 results

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Page 1
Case definition and classification of leukodystrophies and leukoencephalopathies.
Vanderver A, Prust M, Tonduti D, Mochel F, Hussey HM, Helman G, Garbern J, Eichler F, Labauge P, Aubourg P, Rodriguez D, Patterson MC, Van Hove JL, Schmidt J, Wolf NI, Boespflug-Tanguy O, Schiffmann R, van der Knaap MS; GLIA Consortium. Vanderver A, et al. Among authors: patterson mc. Mol Genet Metab. 2015 Apr;114(4):494-500. doi: 10.1016/j.ymgme.2015.01.006. Epub 2015 Jan 29. Mol Genet Metab. 2015. PMID: 25649058 Free PMC article. Review.
Pompe disease diagnosis and management guideline.
Kishnani PS, Steiner RD, Bali D, Berger K, Byrne BJ, Case LE, Crowley JF, Downs S, Howell RR, Kravitz RM, Mackey J, Marsden D, Martins AM, Millington DS, Nicolino M, O'Grady G, Patterson MC, Rapoport DM, Slonim A, Spencer CT, Tifft CJ, Watson MS. Kishnani PS, et al. Among authors: patterson mc. Genet Med. 2006 May;8(5):267-88. doi: 10.1097/01.gim.0000218152.87434.f3. Genet Med. 2006. PMID: 16702877 Free PMC article. No abstract available.
International clinical guidelines for the management of phosphomannomutase 2-congenital disorders of glycosylation: Diagnosis, treatment and follow up.
Altassan R, Péanne R, Jaeken J, Barone R, Bidet M, Borgel D, Brasil S, Cassiman D, Cechova A, Coman D, Corral J, Correia J, de la Morena-Barrio ME, de Lonlay P, Dos Reis V, Ferreira CR, Fiumara A, Francisco R, Freeze H, Funke S, Gardeitchik T, Gert M, Girad M, Giros M, Grünewald S, Hernández-Caselles T, Honzik T, Hutter M, Krasnewich D, Lam C, Lee J, Lefeber D, Marques-de-Silva D, Martinez AF, Moravej H, Õunap K, Pascoal C, Pascreau T, Patterson M, Quelhas D, Raymond K, Sarkhail P, Schiff M, Seroczyńska M, Serrano M, Seta N, Sykut-Cegielska J, Thiel C, Tort F, Vals MA, Videira P, Witters P, Zeevaert R, Morava E. Altassan R, et al. Among authors: patterson m. J Inherit Metab Dis. 2019 Jan;42(1):5-28. doi: 10.1002/jimd.12024. J Inherit Metab Dis. 2019. PMID: 30740725
Consensus clinical management guidelines for Niemann-Pick disease type C.
Geberhiwot T, Moro A, Dardis A, Ramaswami U, Sirrs S, Marfa MP, Vanier MT, Walterfang M, Bolton S, Dawson C, Héron B, Stampfer M, Imrie J, Hendriksz C, Gissen P, Crushell E, Coll MJ, Nadjar Y, Klünemann H, Mengel E, Hrebicek M, Jones SA, Ory D, Bembi B, Patterson M; International Niemann-Pick Disease Registry (INPDR). Geberhiwot T, et al. Among authors: patterson m. Orphanet J Rare Dis. 2018 Apr 6;13(1):50. doi: 10.1186/s13023-018-0785-7. Orphanet J Rare Dis. 2018. PMID: 29625568 Free PMC article. Review.
Neurological Complications of Measles (Rubeola).
Patterson MC. Patterson MC. Curr Neurol Neurosci Rep. 2020 Feb 7;20(2):2. doi: 10.1007/s11910-020-1023-y. Curr Neurol Neurosci Rep. 2020. PMID: 32034528 Review.
Niemann-Pick Disease Type C.
Patterson M. Patterson M. 2000 Jan 26 [updated 2020 Dec 10]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. 2000 Jan 26 [updated 2020 Dec 10]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. PMID: 20301473 Free Books & Documents. Review.
Quo vadis now: Beyond genomics to an era of personalised medicine.
Rahman S, Baumgartner M, Morava E, Patterson M, Peters V, Zschocke J. Rahman S, et al. Among authors: patterson m. J Inherit Metab Dis. 2022 Mar;45(2):129-131. doi: 10.1002/jimd.12487. Epub 2022 Feb 28. J Inherit Metab Dis. 2022. PMID: 35229313 No abstract available.
1,978 results