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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 181
2010 217
2011 246
2012 220
2013 225
2014 218
2015 246
2016 263
2017 218
2018 243
2019 218
2020 259
2021 249
2022 228
2023 225
2024 105

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6,903 results

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Page 1
Gaucher's Disease.
Suner L, Delhommeau F. Suner L, et al. N Engl J Med. 2022 May 19;386(20):1932. doi: 10.1056/NEJMicm2116167. N Engl J Med. 2022. PMID: 35584158 No abstract available.
Gaucher's disease.
Beutler E. Beutler E. N Engl J Med. 1991 Nov 7;325(19):1354-60. doi: 10.1056/NEJM199111073251906. N Engl J Med. 1991. PMID: 1922238 Review. No abstract available.
Gaucher's disease and pregnancy.
Fasouliotis SJ, Ezra Y, Schenker JG. Fasouliotis SJ, et al. Am J Perinatol. 1998 May;15(5):311-8. doi: 10.1055/s-2007-993950. Am J Perinatol. 1998. PMID: 9643638 Review.
Gaucher's disease is an autosomal recessive lysosomal storage disease, resulting from a deficiency of the enzyme glucocerebrosidase, which is required for the lysosomal degradation of glycolipids. ...We present an extensive review of the current litera …
Gaucher's disease is an autosomal recessive lysosomal storage disease, resulting from a deficiency of the enzyme …
Gaucher's disease: report of 11 cases with review of literature.
Essabar L, Meskini T, Lamalmi N, Ettair S, Erreimi N, Mouane N. Essabar L, et al. Pan Afr Med J. 2015 Jan 7;20:18. doi: 10.11604/pamj.2015.20.18.4112. eCollection 2015. Pan Afr Med J. 2015. PMID: 25995815 Free PMC article. Review.
Gaucher's disease (GD) is a lysosomal storage disorder due to glucocerebrosidase deficiency; it's one of the rare genetic diseases for which therapy is now available. ...The visceral symptoms were serious and the neurological features included seizures, hyper …
Gaucher's disease (GD) is a lysosomal storage disorder due to glucocerebrosidase deficiency; it's one of the rare genet …
Gaucher's disease and cancer: a sphingolipid perspective.
Barth BM, Shanmugavelandy SS, Tacelosky DM, Kester M, Morad SA, Cabot MC. Barth BM, et al. Crit Rev Oncog. 2013;18(3):221-34. doi: 10.1615/critrevoncog.2013005814. Crit Rev Oncog. 2013. PMID: 23510065 Free PMC article. Review.
Some suggest that the effects of Gaucher's disease may be linked to cancer, while others implicate the therapies used to treat Gaucher's disease. ...This review should reveal that it is most practical to associate elevated glucosylceramid …
Some suggest that the effects of Gaucher's disease may be linked to cancer, while others implicate the therapies used t …
Gaucher's disease: a review.
Morales LE. Morales LE. Ann Pharmacother. 1996 Apr;30(4):381-8. doi: 10.1177/106002809603000411. Ann Pharmacother. 1996. PMID: 8729893 Review.
OBJECTIVE: To review the epidemiology, pathophysiology, clinical features, diagnosis, and treatment of Gaucher's disease, focusing on the role of enzyme replacement therapy. ...CONCLUSIONS: Enzyme replacement therapy is available for the treatment of type 1 …
OBJECTIVE: To review the epidemiology, pathophysiology, clinical features, diagnosis, and treatment of Gaucher's disease …
Gaucher's Disease. Pathological features.
Pastores GM. Pastores GM. Baillieres Clin Haematol. 1997 Dec;10(4):739-49. doi: 10.1016/s0950-3536(97)80037-6. Baillieres Clin Haematol. 1997. PMID: 9497861 Review.
Gaucher's disease is the most common lysosomal storage disease. The pathological features are a consequence of the progressive accumulation of glucosylceramide within mononuclear phagocytes. ...The general clinico-pathological features of Gaucher …
Gaucher's disease is the most common lysosomal storage disease. The pathological features are a consequence of t …
Gaucher's disease.
Patel AL, Shaikh WA, Khobragade AK, Soni HG, Joshi AS, Sahasrabudhe GS, Chole PV. Patel AL, et al. J Assoc Physicians India. 2009 May;57:410-1. J Assoc Physicians India. 2009. PMID: 19634291
Gaucher's disease is the most common group of lysosomal storage disorders caused by defective activity of an enzyme beta-glucosidase leading to accumulation of glucocerebroside in cells of macrophage lineage. ...Serum beta=glucosidase levels <15% of mean n …
Gaucher's disease is the most common group of lysosomal storage disorders caused by defective activity of an enzyme bet …
Gaucher's disease: past, present and future.
Brady RO. Brady RO. Baillieres Clin Haematol. 1997 Dec;10(4):621-34. doi: 10.1016/s0950-3536(97)80031-5. Baillieres Clin Haematol. 1997. PMID: 9497855 Review.
A patient with what is now known as Gaucher's disease was first described by P.C.E. Gaucher in 1882. Fifty years later, Aghion reported that patients with this condition accumulated a sphingoglycolipid called glucocerebroside. ...Evidence was presented …
A patient with what is now known as Gaucher's disease was first described by P.C.E. Gaucher in 1882. Fifty years …
Gaucher's disease in pregnancy.
Rosnes JS, Sharkey MF, Veille JC, Mueller-Heubach E. Rosnes JS, et al. Obstet Gynecol Surv. 1996 Sep;51(9):549-58. doi: 10.1097/00006254-199609000-00022. Obstet Gynecol Surv. 1996. PMID: 8873155 Review.
Similarly, the genetic variability of Gaucher's disease is diverse, and in some aspects affects phenotypic expression. ...Although pregnancy concurrent with Gaucher's disease has been reported in the medical literature, only one small ser …
Similarly, the genetic variability of Gaucher's disease is diverse, and in some aspects affects phenotypic expression. …
6,903 results