Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1944 1
1945 18
1946 79
1947 76
1948 95
1949 91
1950 164
1951 236
1952 195
1953 216
1954 229
1955 216
1956 203
1957 200
1958 208
1959 180
1960 187
1961 235
1962 236
1963 247
1964 346
1965 320
1966 247
1967 377
1968 381
1969 381
1970 360
1971 366
1972 416
1973 312
1974 400
1975 360
1976 316
1977 366
1978 307
1979 318
1980 309
1981 317
1982 362
1983 328
1984 376
1985 422
1986 394
1987 405
1988 529
1989 428
1990 420
1991 456
1992 375
1993 505
1994 487
1995 563
1996 532
1997 511
1998 567
1999 565
2000 575
2001 615
2002 577
2003 567
2004 569
2005 657
2006 657
2007 725
2008 688
2009 690
2010 795
2011 878
2012 902
2013 961
2014 990
2015 980
2016 927
2017 885
2018 897
2019 893
2020 934
2021 1000
2022 896
2023 713
2024 219

Text availability

Article attribute

Article type

Publication date

Search Results

34,672 results

Results by year

Filters applied: . Clear all
Page 1
Mucopolysaccharidosis IVA: Diagnosis, Treatment, and Management.
Sawamoto K, Álvarez González JV, Piechnik M, Otero FJ, Couce ML, Suzuki Y, Tomatsu S. Sawamoto K, et al. Int J Mol Sci. 2020 Feb 23;21(4):1517. doi: 10.3390/ijms21041517. Int J Mol Sci. 2020. PMID: 32102177 Free PMC article. Review.
Mucopolysaccharidosis type IVA (MPS IVA, or Morquio syndrome type A) is an inherited metabolic lysosomal disease caused by the deficiency of the N-acetylglucosamine-6-sulfate sulfatase enzyme. ...
Mucopolysaccharidosis type IVA (MPS IVA, or Morquio syndrome type A) is an inherited metabolic lysosomal disease caused by the defici
The chondrodystrophies.
Rimoin DL. Rimoin DL. Adv Hum Genet. 1975;5:1-118. doi: 10.1007/978-1-4615-9068-2_1. Adv Hum Genet. 1975. PMID: 805512 Review. No abstract available.
Spondylo-epi-metaphyseal dysplasia.
Cormier-Daire V. Cormier-Daire V. Best Pract Res Clin Rheumatol. 2008 Mar;22(1):33-44. doi: 10.1016/j.berh.2007.12.009. Best Pract Res Clin Rheumatol. 2008. PMID: 18328979 Review.
Saber-sheath Tracheal Deformity.
Kandil A, Chutipongtanate A, Wood RE, Mahmoud M. Kandil A, et al. Anesthesiology. 2018 Oct;129(4):811. doi: 10.1097/ALN.0000000000002268. Anesthesiology. 2018. PMID: 29771708 Free article. No abstract available.
Mucopolysaccharidosis IVA and glycosaminoglycans.
Khan S, Alméciga-Díaz CJ, Sawamoto K, Mackenzie WG, Theroux MC, Pizarro C, Mason RW, Orii T, Tomatsu S. Khan S, et al. Mol Genet Metab. 2017 Jan-Feb;120(1-2):78-95. doi: 10.1016/j.ymgme.2016.11.007. Epub 2016 Nov 29. Mol Genet Metab. 2017. PMID: 27979613 Free PMC article. Review.
Mucopolysaccharidosis IVA (MPS IVA; Morquio A: OMIM 253000) is a lysosomal storage disease with an autosomal recessive trait caused by the deficiency of N-acetylgalactosamine-6-sulfate sulfatase. ...
Mucopolysaccharidosis IVA (MPS IVA; Morquio A: OMIM 253000) is a lysosomal storage disease with an autosomal recessive trait caused b
Thanatophoric dwarfism.
Kaufman RL, Rimoin DL, McAlister WH, Kissane JM. Kaufman RL, et al. Am J Dis Child. 1970 Jul;120(1):53-7. doi: 10.1001/archpedi.1970.02100060087013. Am J Dis Child. 1970. PMID: 4987261 No abstract available.
Diagnosing mucopolysaccharidosis IVA.
Wood TC, Harvey K, Beck M, Burin MG, Chien YH, Church HJ, D'Almeida V, van Diggelen OP, Fietz M, Giugliani R, Harmatz P, Hawley SM, Hwu WL, Ketteridge D, Lukacs Z, Miller N, Pasquali M, Schenone A, Thompson JN, Tylee K, Yu C, Hendriksz CJ. Wood TC, et al. J Inherit Metab Dis. 2013 Mar;36(2):293-307. doi: 10.1007/s10545-013-9587-1. Epub 2013 Feb 1. J Inherit Metab Dis. 2013. PMID: 23371450 Free PMC article.
Mucopolysaccharidosis IVA (MPS IVA; Morquio A syndrome) is an autosomal recessive lysosomal storage disorder resulting from a deficiency of N-acetylgalactosamine-6-sulfate sulfatase (GALNS) activity. ...
Mucopolysaccharidosis IVA (MPS IVA; Morquio A syndrome) is an autosomal recessive lysosomal storage disorder resulting from a deficie
Chondro-osteodystrophy. ? Morquio.
Cholmeley JA. Cholmeley JA. Proc R Soc Med. 1947 Jul;40(9):491. Proc R Soc Med. 1947. PMID: 19993598 Free PMC article. No abstract available.
[Osteochondrodystrophy].
MALAGON-CASTRO V. MALAGON-CASTRO V. Rev Colomb Pediatr Pueric. 1955 Aug-Sep;14(6):441-70. Rev Colomb Pediatr Pueric. 1955. PMID: 13290174 Spanish. No abstract available.
34,672 results
You have reached the last available page of results. Please see the User Guide for more information.