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

Year Number of Results
1930 1
1945 3
1946 11
1947 11
1948 9
1949 13
1950 18
1951 26
1952 22
1953 26
1954 46
1955 35
1956 32
1957 50
1958 33
1959 23
1960 44
1961 53
1962 35
1963 66
1964 47
1965 56
1966 29
1967 42
1968 27
1969 34
1970 42
1971 50
1972 28
1973 32
1974 26
1975 37
1976 43
1977 29
1978 33
1979 29
1980 41
1981 26
1982 29
1983 24
1984 32
1985 45
1986 28
1987 29
1988 46
1989 42
1990 47
1991 49
1992 43
1993 46
1994 45
1995 51
1996 43
1997 43
1998 63
1999 50
2000 56
2001 44
2002 52
2003 54
2004 57
2005 73
2006 85
2007 83
2008 115
2009 93
2010 134
2011 144
2012 145
2013 159
2014 166
2015 160
2016 149
2017 176
2018 190
2019 170
2020 217
2021 221
2022 209
2023 206
2024 176
2025 150

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5,005 results

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Page 1
Bedbugs.
Freedman A, McDougall L, Lamy P. Freedman A, et al. CMAJ. 2023 May 23;195(20):E709. doi: 10.1503/cmaj.221454. CMAJ. 2023. PMID: 37220928 Free PMC article. No abstract available.
Maroteaux-Lamy syndrome.
Lakhotia S, Sharma A, Shrivastava GP, Jain SK. Lakhotia S, et al. Indian J Pediatr. 2004 Oct;71(10):933-5. doi: 10.1007/BF02830840. Indian J Pediatr. 2004. PMID: 15531839
Mucopolysaccharidoses are a type of lysosomal storage disorders characterized by defect in the degradation of Mucopolysaccharides due to deficiency of specific lysosomal enzymes leading to their accumulation in various tissues. MPS -VI (Maroteaux-Lamy Syndrome) is an autos …
Mucopolysaccharidoses are a type of lysosomal storage disorders characterized by defect in the degradation of Mucopolysaccharides due to def …
Punaises de lit.
Freedman A, McDougall L, Lamy P. Freedman A, et al. CMAJ. 2023 Jul 31;195(29):E996-E997. doi: 10.1503/cmaj.221454-f. CMAJ. 2023. PMID: 37524398 Free PMC article. French. No abstract available.
Autoimmune neutropenia.
Autrel-Moignet A, Lamy T. Autrel-Moignet A, et al. Presse Med. 2014 Apr;43(4 Pt 2):e105-18. doi: 10.1016/j.lpm.2014.02.007. Epub 2014 Mar 27. Presse Med. 2014. PMID: 24680423 Review.
Atlantoaxial instability in a case of Maroteaux-Lamy syndrome.
Shah A, Jadhav N, Dandpat S, Goel A. Shah A, et al. J Craniovertebr Junction Spine. 2021 Jan-Mar;12(1):91-94. doi: 10.4103/jcvjs.JCVJS_5_21. Epub 2021 Mar 4. J Craniovertebr Junction Spine. 2021. PMID: 33850389 Free PMC article.
A relatively rare report of an 8-year-old girl with Maroteaux-Lamy syndrome that is Type VI mucopolysaccharidosis who presented with symptoms of spastic quadriparesis related to atlantoaxial instability is presented. ...
A relatively rare report of an 8-year-old girl with Maroteaux-Lamy syndrome that is Type VI mucopolysaccharidosis who presented with …
Multilevel myelopathy in Maroteaux-Lamy syndrome and review of the literature.
Mut M, Cila A, Varli K, Akalan N. Mut M, et al. Clin Neurol Neurosurg. 2005 Apr;107(3):230-5. doi: 10.1016/j.clineuro.2004.05.003. Clin Neurol Neurosurg. 2005. PMID: 15823680 Review.
An 18-year-old male with Maroteaux-Lamy syndrome was presented with spastic quadriparesis. Magnetic resonance imaging of whole spinal canal revealed stenosis at multiple levels of cervical, thoracic and lumbar regions. ...The etiology of myelopathy and priority of the leve …
An 18-year-old male with Maroteaux-Lamy syndrome was presented with spastic quadriparesis. Magnetic resonance imaging of whole spinal …
Neurosurgical interventions in children with Maroteaux-Lamy syndrome. Case report and review of the literature.
Vougioukas VI, Berlis A, Kopp MV, Korinthenberg R, Spreer J, van Velthoven V. Vougioukas VI, et al. Pediatr Neurosurg. 2001 Jul;35(1):35-8. doi: 10.1159/000050383. Pediatr Neurosurg. 2001. PMID: 11490189 Review.
This paper reports the case of a 14-year-old child with Maroteaux-Lamy syndrome (mucopolysaccharidosis type 6) who was treated consecutively for compressive damage of the optic nerves, hydrocephalus communicans and progressive spastic tetraparesis within 2 years. The clini …
This paper reports the case of a 14-year-old child with Maroteaux-Lamy syndrome (mucopolysaccharidosis type 6) who was treated consec …
[Maroteaux-Lamy syndrome: a case report].
Mtar A, Charfeddine B, Braham I, Ben Abdallah J, Neffati S, Smach MA, Bourfifa Z, Ksouri M, Dridi H, Limem K. Mtar A, et al. Ann Biol Clin (Paris). 2011 Nov-Dec;69(6):693-7. doi: 10.1684/abc.2011.0627. Ann Biol Clin (Paris). 2011. PMID: 22123570 Free article. French.
The Maroteaux-Lamy disease, or mucopolysaccharidosis type VI is an inherited metabolic disorder severe and rare. ...Hence the diagnosis of syndrome Maroteaux-Lamy in its mild form (type B) was selected....
The Maroteaux-Lamy disease, or mucopolysaccharidosis type VI is an inherited metabolic disorder severe and rare. ...Hence the diagnos …
5,005 results