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

Year Number of Results
1985 1
1993 1
1995 1
1996 1
1997 1
1998 1
1999 1
2000 2
2001 1
2002 2
2005 2
2007 1
2008 2
2009 5
2010 2
2012 1
2013 1
2014 1
2015 3
2016 2
2017 5
2018 5
2019 4
2020 1
2021 3
2022 0
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43 results
Results by year
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Page 1
Newborn screening for Krabbe disease in New York State: the first eight years' experience.
Orsini JJ, Kay DM, Saavedra-Matiz CA, Wenger DA, Duffner PK, Erbe RW, Biski C, Martin M, Krein LM, Nichols M, Kurtzberg J, Escolar ML, Adams DJ, Arnold GL, Iglesias A, Galvin-Parton P, Kronn DF, Kwon JM, Levy PA, Pellegrino JE, Shur N, Wasserstein MP, Caggana M; New York State Krabbe Disease Consortium. Orsini JJ, et al. Among authors: kronn df. Genet Med. 2016 Mar;18(3):239-48. doi: 10.1038/gim.2015.211. Epub 2016 Jan 21. Genet Med. 2016. PMID: 26795590
Pain Phenotypes in Rare Musculoskeletal and Neuromuscular Diseases.
Tucker-Bartley A, Lemme J, Gomez-Morad A, Shah N, Veliu M, Birklein F, Storz C, Rutkove S, Kronn D, Boyce AM, Kraft E, Upadhyay J. Tucker-Bartley A, et al. Among authors: kronn d. Neurosci Biobehav Rev. 2021 May;124:267-290. doi: 10.1016/j.neubiorev.2021.02.009. Epub 2021 Feb 10. Neurosci Biobehav Rev. 2021. PMID: 33581222 Review.
Hereditary Folate Malabsorption.
Kronn D, Goldman ID. Kronn D, et al. 2008 Jun 17 [updated 2017 Apr 27]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Mirzaa GM, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. 2008 Jun 17 [updated 2017 Apr 27]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Mirzaa GM, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. PMID: 20301716 Free Books & Documents. Review.
Cardiac responses in paediatric Pompe disease in the ADVANCE patient cohort.
Byrne BJ, Colan SD, Kishnani PS, Foster MC, Sparks SE, Gibson JB, An Haack K, Stockton DW, Peña LDM, Hahn SH, Johnson J, Tanpaiboon PX, Leslie ND, Kronn D, Hillman RE, Wang RY; Pompe ADVANCE Study Consortium. Byrne BJ, et al. Among authors: kronn d. Cardiol Young. 2021 Aug 23:1-10. doi: 10.1017/S1047951121002079. Online ahead of print. Cardiol Young. 2021. PMID: 34420548
A Delphi-based consensus clinical practice protocol for the diagnosis and management of 3-methylcrotonyl CoA carboxylase deficiency.
Arnold GL, Koeberl DD, Matern D, Barshop B, Braverman N, Burton B, Cederbaum S, Fiegenbaum A, Garganta C, Gibson J, Goodman SI, Harding C, Kahler S, Kronn D, Longo N. Arnold GL, et al. Among authors: kronn d. Mol Genet Metab. 2008 Apr;93(4):363-70. doi: 10.1016/j.ymgme.2007.11.002. Epub 2007 Dec 21. Mol Genet Metab. 2008. PMID: 18155630
Schwannomatosis: a clinical and pathologic study.
MacCollin M, Woodfin W, Kronn D, Short MP. MacCollin M, et al. Among authors: kronn d. Neurology. 1996 Apr;46(4):1072-9. doi: 10.1212/wnl.46.4.1072. Neurology. 1996. PMID: 8780094 Review.
Phosphoglucomutase-1 deficiency: Early presentation, metabolic management and detection in neonatal blood spots.
Conte F, Morava E, Bakar NA, Wortmann SB, Poerink AJ, Grunewald S, Crushell E, Al-Gazali L, de Vries MC, Mørkrid L, Hertecant J, Brocke Holmefjord KS, Kronn D, Feigenbaum A, Fingerhut R, Wong SY, van Scherpenzeel M, Voermans NC, Lefeber DJ. Conte F, et al. Among authors: kronn d. Mol Genet Metab. 2020 Sep-Oct;131(1-2):135-146. doi: 10.1016/j.ymgme.2020.08.003. Epub 2020 Sep 17. Mol Genet Metab. 2020. PMID: 33342467 Free article.
43 results