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

Year Number of Results
1979 1
1981 2
1982 1
1983 5
1984 5
1985 1
1986 4
1987 4
1988 2
1989 1
1990 3
1991 5
1992 2
1993 10
1994 6
1995 3
1996 6
1997 1
1998 10
1999 12
2000 10
2001 11
2002 18
2003 11
2004 6
2005 7
2006 8
2007 8
2008 11
2009 9
2010 9
2011 9
2012 11
2013 13
2014 13
2015 7
2016 6
2017 9
2018 11
2019 11
2020 18
2021 18
2022 20
2023 26
2024 7

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PubMed for id: 78644

335 results

Results by year

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Page 1
Neutrophil functions in patients with neutropenia due to glycogen storage disease type 1b treated with empagliflozin.
Kaczor M, Malicki S, Folkert J, Dobosz E, Bryzek D, Chruścicka-Smaga B, Greczan M, Wesół-Kucharska D, Piatosa B Prof, Samborowska E, Madzio J, Książyk J, Vel Emczyńska EE, Hajdacka M, Potempa J, Młynarski W, Rokicki D, Veillard F. Kaczor M, et al. Blood Adv. 2024 Mar 26:bloodadvances.2023012403. doi: 10.1182/bloodadvances.2023012403. Online ahead of print. Blood Adv. 2024. PMID: 38531056
Treatment recommendations for glycogen storage disease type IB- associated neutropenia and neutrophil dysfunction with empagliflozin: Consensus from an international workshop.
Grünert SC, Derks TGJ, Mundy H, Dalton RN, Donadieu J, Hofbauer P, Jones N, Uçar SK, LaFreniere J, Contreras EL, Pendyal S, Rossi A, Schneider B, Spiegel R, Stepien KM, Wesol-Kucharska D, Veiga-da-Cunha M, Wortmann SB. Grünert SC, et al. Mol Genet Metab. 2024 Mar;141(3):108144. doi: 10.1016/j.ymgme.2024.108144. Epub 2024 Jan 17. Mol Genet Metab. 2024. PMID: 38277989 Free article. Review.
Hepatic ChREBP orchestrates intrahepatic carbohydrate metabolism to limit hepatic glucose 6-phosphate and glycogen accumulation in a mouse model for acute Glycogen Storage Disease type Ib.
Krishnamurthy KA, Rutten MGS, Hoogerland JA, van Dijk TH, Bos T, Koehorst M, de Vries MP, Kloosterhuis NJ, Havinga H, Schomakers BV, van Weeghel M, Wolters JC, Bakker BM, Oosterveer MH. Krishnamurthy KA, et al. Mol Metab. 2024 Jan;79:101838. doi: 10.1016/j.molmet.2023.101838. Epub 2023 Nov 22. Mol Metab. 2024. PMID: 37995884 Free PMC article.
Assessment of the diagnosis, treatment, and follow-up of a group of Turkish pediatric glycogen storage disease type 1b patients with varying clinical presentations and a novel mutation.
Küçükçongar Yavaş A, Engin Erdal A, Bilginer Gürbüz B, Ünlüsoy Aksu A, Kasapkara ÇS. Küçükçongar Yavaş A, et al. J Pediatr Endocrinol Metab. 2023 Oct 5;36(11):1092-1099. doi: 10.1515/jpem-2023-0336. Print 2023 Nov 27. J Pediatr Endocrinol Metab. 2023. PMID: 37791580
335 results