PubMed (Bookshelf cited) for id: 82815

Year	Number of Results
1969	1
1999	1
2000	2
2001	2
2003	2
2004	1
2006	2
2007	3
2008	3
2009	2
2010	1
2011	1
2012	3
2013	5
2014	2
2015	3
2016	3
2017	3
2018	5
2019	6
2023	0

1

Chronic liver involvement in urea cycle disorders.

Ranucci G, Rigoldi M, Cotugno G, Bernabei SM, Liguori A, Gasperini S, Goffredo BM, Martinelli D, Monti L, Francalanci P, Candusso M, Parini R, Dionisi-Vici C. Ranucci G, et al. J Inherit Metab Dis. 2019 Nov;42(6):1118-1127. doi: 10.1002/jimd.12144. Epub 2019 Aug 25. J Inherit Metab Dis. 2019. PMID: 31260111

2

Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome in pregnancy: Considerations for management and review of the literature.

Ho B, MacKenzie J, Walia J, Geraghty M, Smith G, Nedvidek J, Guerin A. Ho B, et al. JIMD Rep. 2019 Mar 14;46(1):28-34. doi: 10.1002/jmd2.12025. eCollection 2019 Mar. JIMD Rep. 2019. PMID: 31240152 Free PMC article.

3

Urea cycle disorders-update.

Matsumoto S, Häberle J, Kido J, Mitsubuchi H, Endo F, Nakamura K. Matsumoto S, et al. J Hum Genet. 2019 Sep;64(9):833-847. doi: 10.1038/s10038-019-0614-4. Epub 2019 May 20. J Hum Genet. 2019. PMID: 31110235 Review.

4

Suggested guidelines for the diagnosis and management of urea cycle disorders: First revision.

Häberle J, Burlina A, Chakrapani A, Dixon M, Karall D, Lindner M, Mandel H, Martinelli D, Pintos-Morell G, Santer R, Skouma A, Servais A, Tal G, Rubio V, Huemer M, Dionisi-Vici C. Häberle J, et al. J Inherit Metab Dis. 2019 Nov;42(6):1192-1230. doi: 10.1002/jimd.12100. Epub 2019 May 15. J Inherit Metab Dis. 2019. PMID: 30982989 Review.

5

Evaluation of dietary treatment and amino acid supplementation in organic acidurias and urea-cycle disorders: On the basis of information from a European multicenter registry.

Molema F, Gleich F, Burgard P, van der Ploeg AT, Summar ML, Chapman KA, Barić I, Lund AM, Kölker S, Williams M; Additional individual contributors from E-IMD. Molema F, et al. J Inherit Metab Dis. 2019 Nov;42(6):1162-1175. doi: 10.1002/jimd.12066. Epub 2019 Feb 27. J Inherit Metab Dis. 2019. PMID: 30734935 Free article.

6

Late onset hyperornithinemia-hyperammonemia-homocitrullinuria syndrome - how web searching by the family solved unexplained unconsciousness: a case report.

Silfverberg T, Sahlander F, Enlund M, Oscarson M, Hårdstedt M. Silfverberg T, et al. J Med Case Rep. 2018 Sep 23;12(1):274. doi: 10.1186/s13256-018-1794-9. J Med Case Rep. 2018. PMID: 30243302 Free PMC article.

7

Hyperornithinemia, Hyperammonemia, and Homocitrullinuria Syndrome Causing Severe Neonatal Hyperammonemia.

Wild KT, Ganetzky RD, Yudkoff M, Ierardi-Curto L. Wild KT, et al. JIMD Rep. 2019;44:103-107. doi: 10.1007/8904_2018_132. Epub 2018 Sep 6. JIMD Rep. 2019. PMID: 30187369 Free PMC article.

8

Lactate/pyruvate in hyperornithinemia-hyperammonemia-homocitrullinuria syndrome.

Ono H, Tamada T, Shigematsu Y. Ono H, et al. Pediatr Int. 2018 Aug;60(8):762-764. doi: 10.1111/ped.13608. Epub 2018 Jul 30. Pediatr Int. 2018. PMID: 30058227 No abstract available.

9

Scales for the clinical evaluation of cerebellar disorders.

Bürk K, Sival DA. Bürk K, et al. Handb Clin Neurol. 2018;154:329-339. doi: 10.1016/B978-0-444-63956-1.00020-5. Handb Clin Neurol. 2018. PMID: 29903450 Review.

10

The Science and Translation of Lactate Shuttle Theory.

Brooks GA. Brooks GA. Cell Metab. 2018 Apr 3;27(4):757-785. doi: 10.1016/j.cmet.2018.03.008. Cell Metab. 2018. PMID: 29617642 Free article. Review.

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