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

Year Number of Results
1986 1
1990 1
1991 2
1992 1
1993 1
1994 2
1995 3
1996 1
2001 3
2002 2
2003 1
2004 2
2005 1
2006 3
2007 1
2008 3
2009 5
2010 5
2011 3
2012 4
2013 2
2014 5
2015 4
2016 2
2018 1
2019 2
2020 1
2021 2
2022 0
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Search Results

61 results
Results by year
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Page 1
Trichohyalin and matrix proteins.
Rogers GE, Fietz MJ, Fratini A. Rogers GE, et al. Among authors: fietz mj. Ann N Y Acad Sci. 1991 Dec 26;642:64-80; discussion 80-1. Ann N Y Acad Sci. 1991. PMID: 1809119 Review. 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. Among authors: fietz m. 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.
β-Mannosidosis in German Shepherd Dogs.
Jolly RD, Dittmer KE, Garrick DJ, Chernyavtseva A, Hemsley KM, King B, Fietz M, Shackleton NM, Fairley R, Wylie K. Jolly RD, et al. Among authors: fietz m. Vet Pathol. 2019 Sep;56(5):743-748. doi: 10.1177/0300985819839239. Epub 2019 Apr 14. Vet Pathol. 2019. PMID: 30983534
Increased Risk of Autopsy-Proven Pneumonia with Sex, Season and Neurodegenerative Disease.
Beach TG, Russell A, Sue LI, Intorcia AJ, Glass MJ, Walker JE, Arce R, Nelson CM, Hidalgo T, Chiarolanza G, Mariner M, Scroggins A, Pullen J, Souders L, Sivananthan K, Carter N, Saxon-LaBelle M, Hoffman B, Garcia A, Callan M, Fornwalt BE, Carew J, Filon J, Cutler B, Papa J, Curry JR, Oliver J, Shprecher D, Atri A, Belden C, Shill HA, Driver-Dunckley E, Mehta SH, Adler CH, Haarer CF, Ruhlen T, Torres M, Nguyen S, Schmitt D, Fietz M, Lue LF, Walker DG, Mizgerd JP, Serrano GE. Beach TG, et al. Among authors: fietz m. medRxiv. 2021 Jan 8:2021.01.07.21249410. doi: 10.1101/2021.01.07.21249410. Preprint. medRxiv. 2021. PMID: 33442709 Free PMC article.
Neuronal ceroid lipofuscinosis type 2: an Australian case series.
Johnson AM, Mandelstam S, Andrews I, Boysen K, Yaplito-Lee J, Fietz M, Nagarajan L, Rodriguez-Casero V, Ryan MM, Smith N, Scheffer IE, Ellaway C. Johnson AM, et al. Among authors: fietz m. J Paediatr Child Health. 2020 Aug;56(8):1210-1218. doi: 10.1111/jpc.14890. Epub 2020 Apr 24. J Paediatr Child Health. 2020. PMID: 32329550 Free PMC article.
What's Wrong with the Transferrin?
Wijeratne N, Tudball R, Choy KW, Fietz M, Doery JC. Wijeratne N, et al. Among authors: fietz m. Clin Chem. 2016 Feb;62(2):413-4. doi: 10.1373/clinchem.2015.241083. Clin Chem. 2016. PMID: 26823612 No abstract available.
Harmonizing the Collection of Clinical Data on Genetic Testing Requisition Forms to Enhance Variant Interpretation in Hypertrophic Cardiomyopathy (HCM): A Study from the ClinGen Cardiomyopathy Variant Curation Expert Panel.
Morales A, Ing A, Antolik C, Austin-Tse C, Baudhuin LM, Bronicki L, Cirino A, Hawley MH, Fietz M, Garcia J, Ho C, Ingles J, Jarinova O, Johnston T, Kelly MA, Kurtz CL, Lebo M, Macaya D, Mahanta L, Maleszewski J, Manrai AK, Murray M, Richard G, Semsarian C, Thomson KL, Winder T, Ware JS, Hershberger RE, Funke BH, Vatta M; ClinGen Cardiovascular Clinical Domain Working Group; Cardiomyopathy Variant Curation Expert Panel. Morales A, et al. Among authors: fietz m. J Mol Diagn. 2021 May;23(5):589-598. doi: 10.1016/j.jmoldx.2021.01.014. Epub 2021 Feb 22. J Mol Diagn. 2021. PMID: 33631351 Free PMC article.
61 results