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

Year Number of Results
1912 1
1926 2
1927 2
1930 1
1931 3
1932 2
1933 2
1934 1
1935 1
1937 1
1938 1
1939 1
1940 2
1941 1
1945 2
1946 5
1947 10
1948 14
1949 13
1950 12
1951 17
1952 17
1953 16
1954 13
1955 10
1956 9
1957 16
1958 15
1959 12
1960 21
1961 26
1962 29
1963 30
1964 35
1965 40
1966 29
1967 46
1968 46
1969 51
1970 49
1971 49
1972 55
1973 56
1974 48
1975 46
1976 45
1977 67
1978 68
1979 51
1980 63
1981 53
1982 101
1983 39
1984 58
1985 74
1986 62
1987 69
1988 62
1989 65
1990 68
1991 79
1992 86
1993 104
1994 102
1995 115
1996 100
1997 126
1998 128
1999 98
2000 105
2001 104
2002 119
2003 111
2004 114
2005 126
2006 171
2007 167
2008 141
2009 180
2010 217
2011 246
2012 220
2013 225
2014 219
2015 246
2016 263
2017 218
2018 243
2019 218
2020 257
2021 246
2022 227
2023 226
2024 224
2025 253
2026 179

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7,408 results

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Page 1
Gaucher Disease for Hematologists.
Özdemir GN, Gündüz E. Özdemir GN, et al. Turk J Haematol. 2022 Jun 1;39(2):136-139. doi: 10.4274/tjh.galenos.2021.2021.0683. Epub 2022 Apr 20. Turk J Haematol. 2022. PMID: 35439918 Free PMC article. Review.
Gaucher disease (GD) is a rare hereditary lysosomal storage disease that arises due to deficiency of glucocerebrosidase. ...
Gaucher disease (GD) is a rare hereditary lysosomal storage disease that arises due to deficiency of glucocerebrosidase …
[Gaucher disease: A review].
Nguyen Y, Stirnemann J, Belmatoug N. Nguyen Y, et al. Rev Med Interne. 2019 May;40(5):313-322. doi: 10.1016/j.revmed.2018.11.012. Epub 2019 Jan 11. Rev Med Interne. 2019. PMID: 30638965 Review. French.
Type 1 Gaucher disease is associated with a higher risk of Parkinson disease, some solid cancers, and hematologic diseases in particularly multiple myeloma. Specific treatment, such as enzyme replacement therapy or substrate reduction therapy is indicated in …
Type 1 Gaucher disease is associated with a higher risk of Parkinson disease, some solid cancers, and hematologic disea …
Gaucher disease.
Butters TD. Butters TD. Curr Opin Chem Biol. 2007 Aug;11(4):412-8. doi: 10.1016/j.cbpa.2007.05.035. Epub 2007 Jul 23. Curr Opin Chem Biol. 2007. PMID: 17644022 Review.
Although Gaucher disease is a rare disorder, recent developments in novel means for therapeutic intervention have invigorated both academic research and pharmaceutical industry discovery programmes. The common mutations found in the lysosomal enzyme deficient in …
Although Gaucher disease is a rare disorder, recent developments in novel means for therapeutic intervention have invigorated …
Gaucher disease.
Mignot C, Gelot A, De Villemeur TB. Mignot C, et al. Handb Clin Neurol. 2013;113:1709-15. doi: 10.1016/B978-0-444-59565-2.00040-X. Handb Clin Neurol. 2013. PMID: 23622393 Review.
Gaucher disease is an autosomal recessive condition due to glucocerebrosidase deficiency responsible for the lysosomal accumulation of glucosylceramide, a complex lipid derived from cell membranes, mainly in macrophages. ...Splenomegaly, blood cytopenia, and bone in …
Gaucher disease is an autosomal recessive condition due to glucocerebrosidase deficiency responsible for the lysosomal accumul …
[Gaucher Disease].
Okuyama T. Okuyama T. Brain Nerve. 2015 Sep;67(9):1109-13. doi: 10.11477/mf.1416200267. Brain Nerve. 2015. PMID: 26329151 Review. Japanese.
Gaucher disease is an autosomal recessive disorder caused by congenital deficiency of lysosomal glucocerebrosidase. Gaucher disease is classified into three types. In addition to enzyme replacement therapy, substrate reduction therapy, chemical chapero …
Gaucher disease is an autosomal recessive disorder caused by congenital deficiency of lysosomal glucocerebrosidase. Gaucher …
Gaucher disease.
Enderlin C, Vogel R, Conaway P. Enderlin C, et al. Am J Nurs. 2003 Dec;103(12):50-60; quiz 61. doi: 10.1097/00000446-200312000-00018. Am J Nurs. 2003. PMID: 14702566 Review. No abstract available.
Gaucher disease: unmet treatment needs.
Mehta A. Mehta A. Acta Paediatr. 2008 Apr;97(457):83-7. doi: 10.1111/j.1651-2227.2008.00653.x. Acta Paediatr. 2008. PMID: 18339195 Review.
Gaucher disease is a multisystemic metabolic disorder arising from a deficiency of lysosomal glucocerebrosidase. ...Potential new treatments for Gaucher disease include small molecules, which may penetrate tissues that are not accessible by ERT. ...
Gaucher disease is a multisystemic metabolic disorder arising from a deficiency of lysosomal glucocerebrosidase. ...Potential …
Editorial: Gaucher disease.
Mikosch P. Mikosch P. Wien Med Wochenschr. 2010 Dec;160(23-24):593. doi: 10.1007/s10354-010-0851-9. Wien Med Wochenschr. 2010. PMID: 21221910 No abstract available.
Gaucher disease: a comprehensive review.
Rosenbloom BE, Weinreb NJ. Rosenbloom BE, et al. Crit Rev Oncog. 2013;18(3):163-75. doi: 10.1615/critrevoncog.2013006060. Crit Rev Oncog. 2013. PMID: 23510062 Review.
Gaucher disease (GD) is an inherited error of metabolism due to a deficiency of glucocerebrosidase. ...This article reviews a broad spectrum of information regarding Gaucher disease, from the history of the disease to newer therapies still in th …
Gaucher disease (GD) is an inherited error of metabolism due to a deficiency of glucocerebrosidase. ...This article reviews a …
Gaucher disease: haematological presentations and complications.
Thomas AS, Mehta A, Hughes DA. Thomas AS, et al. Br J Haematol. 2014 May;165(4):427-40. doi: 10.1111/bjh.12804. Epub 2014 Mar 3. Br J Haematol. 2014. PMID: 24588457 Review.
Gaucher disease (GD) is an autosomal recessive lysosomal storage disease, caused by deficiency of the enzyme glucocerebrosidase, required for the degradation of glycosphingolipids. Clinical manifestations include hepatosplenomegaly, thrombocytopenia, bone …
Gaucher disease (GD) is an autosomal recessive lysosomal storage disease, caused by deficiency of the enzyme glucocereb …
7,408 results