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

Year Number of Results
1949 1
1950 1
1951 1
1953 1
1966 1
1968 6
1969 5
1970 3
1971 10
1972 6
1973 6
1974 7
1975 6
1976 4
1977 3
1981 2
1982 6
1983 4
1984 6
1985 5
1986 3
1987 2
1988 7
1989 3
1990 5
1991 5
1992 4
1993 8
1994 7
1995 5
1996 8
1997 6
1998 4
1999 8
2000 11
2001 3
2002 4
2003 13
2004 9
2005 8
2006 7
2007 8
2008 1
2009 4
2010 4
2011 3
2012 2
2013 2
2014 3
2015 3
2016 4
2017 4
2018 1
2019 1
2020 2
2021 1
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250 results
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Page 1
Canavan Disease.
Matalon R, Delgado L, Michals-Matalon K. Matalon R, et al. 1999 Sep 16 [updated 2018 Sep 13]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Mirzaa G, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2021. 1999 Sep 16 [updated 2018 Sep 13]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Mirzaa G, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2021. PMID: 20301412 Free Books & Documents. Review.
Multiple phenotypes in phosphoglucomutase 1 deficiency.
Tegtmeyer LC, Rust S, van Scherpenzeel M, Ng BG, Losfeld ME, Timal S, Raymond K, He P, Ichikawa M, Veltman J, Huijben K, Shin YS, Sharma V, Adamowicz M, Lammens M, Reunert J, Witten A, Schrapers E, Matthijs G, Jaeken J, Rymen D, Stojkovic T, Laforêt P, Petit F, Aumaître O, Czarnowska E, Piraud M, Podskarbi T, Stanley CA, Matalon R, Burda P, Seyyedi S, Debus V, Socha P, Sykut-Cegielska J, van Spronsen F, de Meirleir L, Vajro P, DeClue T, Ficicioglu C, Wada Y, Wevers RA, Vanderschaeghe D, Callewaert N, Fingerhut R, van Schaftingen E, Freeze HH, Morava E, Lefeber DJ, Marquardt T. Tegtmeyer LC, et al. Among authors: matalon r. N Engl J Med. 2014 Feb 6;370(6):533-42. doi: 10.1056/NEJMoa1206605. N Engl J Med. 2014. PMID: 24499211 Free PMC article.
Identification of novel candidate disease genes from de novo exonic copy number variants.
Gambin T, Yuan B, Bi W, Liu P, Rosenfeld JA, Coban-Akdemir Z, Pursley AN, Nagamani SCS, Marom R, Golla S, Dengle L, Petrie HG, Matalon R, Emrick L, Proud MB, Treadwell-Deering D, Chao HT, Koillinen H, Brown C, Urraca N, Mostafavi R, Bernes S, Roeder ER, Nugent KM, Bader PI, Bellus G, Cummings M, Northrup H, Ashfaq M, Westman R, Wildin R, Beck AE, Immken L, Elton L, Varghese S, Buchanan E, Faivre L, Lefebvre M, Schaaf CP, Walkiewicz M, Yang Y, Kang SL, Lalani SR, Bacino CA, Beaudet AL, Breman AM, Smith JL, Cheung SW, Lupski JR, Patel A, Shaw CA, Stankiewicz P. Gambin T, et al. Among authors: matalon r. Genome Med. 2017 Sep 21;9(1):83. doi: 10.1186/s13073-017-0472-7. Genome Med. 2017. PMID: 28934986 Free PMC article.
Cell-Based Therapy for Canavan Disease Using Human iPSC-Derived NPCs and OPCs.
Feng L, Chao J, Tian E, Li L, Ye P, Zhang M, Chen X, Cui Q, Sun G, Zhou T, Felix G, Qin Y, Li W, Meza ED, Klein J, Ghoda L, Hu W, Luo Y, Dang W, Hsu D, Gold J, Goldman SA, Matalon R, Shi Y. Feng L, et al. Among authors: matalon r. Adv Sci (Weinh). 2020 Oct 29;7(23):2002155. doi: 10.1002/advs.202002155. eCollection 2020 Dec. Adv Sci (Weinh). 2020. PMID: 33304759 Free PMC article.
Fragile X syndrome.
Hayes EW, Matalon R. Hayes EW, et al. Among authors: matalon r. Pediatrics. 2009 Aug;124(2):790-2. doi: 10.1542/peds.2009-0569. Epub 2009 Jul 5. Pediatrics. 2009. PMID: 19581265 No abstract available.
Trends in enzyme therapy for phenylketonuria.
Kim W, Erlandsen H, Surendran S, Stevens RC, Gamez A, Michols-Matalon K, Tyring SK, Matalon R. Kim W, et al. Among authors: matalon r. Mol Ther. 2004 Aug;10(2):220-4. doi: 10.1016/j.ymthe.2004.05.001. Mol Ther. 2004. PMID: 15294168 Free article. Review.
The Hurler and Hunter syndromes.
Dorfman A, Matalon R. Dorfman A, et al. Among authors: matalon r. Am J Med. 1969 Nov;47(5):691-707. doi: 10.1016/0002-9343(69)90164-8. Am J Med. 1969. PMID: 4243120 Review. No abstract available.
Prenatal diagnosis of Canavan disease.
Matalon R, Michals-Matalon K. Matalon R, et al. Prenat Diagn. 1999 Jul;19(7):669-70. doi: 10.1002/(sici)1097-0223(199907)19:7<669::aid-pd630>3.0.co;2-n. Prenat Diagn. 1999. PMID: 10419617 Review. No abstract available.
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