Herasse M[au] - Search Results

Year	Number of Results
1999	1
2000	2
2001	1
2002	2
2003	2
2005	1
2006	2
2007	1
2009	1
2021	1
2022	0

1

[Transition from pediatric to adult care: Recommendations of the French network for autoimmune and autoinflammatory diseases (FAI²R)].

Georgin-Lavialle S, Hentgen V, Truchetet ME, Romier M, Hérasse M, Maillard H, Pha M, Pillet P, Reumaux H, Duquesne A, Larbre JP, Belot A. Georgin-Lavialle S, et al. Among authors: herasse m. Rev Med Interne. 2021 Sep;42(9):633-638. doi: 10.1016/j.revmed.2021.02.003. Epub 2021 Jun 17. Rev Med Interne. 2021. PMID: 34147259 French.

2

Clinical and histopathological aspects of central core disease associated and non-associated with RYR1 locus.

Romero NB, Herasse M, Monnier N, Leroy JP, Fischer D, Ferreiro A, Viollet L, Eymard B, Laforêt P, Monges S, Lubieniecki F, Taratuto AL, Guicheney P, Lunardi J, Fardeau M. Romero NB, et al. Among authors: herasse m. Acta Myol. 2005 Oct;24(2):70-3. Acta Myol. 2005. PMID: 16550918 Review.

3

Alteration of sarcoplasmic reticulum ca release in skeletal muscle from calpain 3-deficient mice.

Dayanithi G, Richard I, Viero C, Mazuc E, Mallie S, Valmier J, Bourg N, Herasse M, Marty I, Lefranc G, Mangeat P, Baghdiguian S. Dayanithi G, et al. Among authors: herasse m. Int J Cell Biol. 2009;2009:340346. doi: 10.1155/2009/340346. Epub 2010 Mar 14. Int J Cell Biol. 2009. PMID: 20300593 Free PMC article.

4

Characterization of the muscle involvement in dynamin 2-related centronuclear myopathy.

Fischer D, Herasse M, Bitoun M, Barragán-Campos HM, Chiras J, Laforêt P, Fardeau M, Eymard B, Guicheney P, Romero NB. Fischer D, et al. Among authors: herasse m. Brain. 2006 Jun;129(Pt 6):1463-9. doi: 10.1093/brain/awl071. Epub 2006 Apr 3. Brain. 2006. PMID: 16585051

5

Abnormal distribution of calcium-handling proteins: a novel distinctive marker in core myopathies.

Herasse M, Parain K, Marty I, Monnier N, Kaindl AM, Leroy JP, Richard P, Lunardi J, Romero NB, Ferreiro A. Herasse M, et al. J Neuropathol Exp Neurol. 2007 Jan;66(1):57-65. doi: 10.1097/NEN.0b013e31802d47ce. J Neuropathol Exp Neurol. 2007. PMID: 17204937

6

Severe hypophosphatasia: characterization of fifteen novel mutations in the ALPL gene.

Spentchian M, Merrien Y, Herasse M, Dobbie Z, Gläser D, Holder SE, Ivarsson SA, Kostiner D, Mansour S, Norman A, Roth J, Stipoljev F, Taillemite JL, van der Smagt JJ, Serre JL, Simon-Bouy B, Taillandier A, Mornet E. Spentchian M, et al. Among authors: herasse m. Hum Mutat. 2003 Jul;22(1):105-6. doi: 10.1002/humu.9159. Hum Mutat. 2003. PMID: 12815606

7

Muscle imaging in dominant core myopathies linked or unlinked to the ryanodine receptor 1 gene.

Fischer D, Herasse M, Ferreiro A, Barragán-Campos HM, Chiras J, Viollet L, Maugenre S, Leroy JP, Monnier N, Lunardi J, Guicheney P, Fardeau M, Romero NB. Fischer D, et al. Among authors: herasse m. Neurology. 2006 Dec 26;67(12):2217-20. doi: 10.1212/01.wnl.0000249151.45200.71. Neurology. 2006. PMID: 17190947

8

Molecular study of three cases of odontohypophosphatasia resulting from heterozygosity for mutations in the tissue non-specific alkaline phosphatase gene.

Herasse M, Spentchian M, Taillandier A, Keppler-Noreuil K, Fliorito AN, Bergoffen J, Wallerstein R, Muti C, Simon-Bouy B, Mornet E. Herasse M, et al. J Med Genet. 2003 Aug;40(8):605-9. doi: 10.1136/jmg.40.8.605. J Med Genet. 2003. PMID: 12920074 Free PMC article. No abstract available.

9

Calpain 3 mRNA expression in mice after denervation and during muscle regeneration.

Stockholm D, Herasse M, Marchand S, Praud C, Roudaut C, Richard I, Sebille A, Beckmann JS. Stockholm D, et al. Among authors: herasse m. Am J Physiol Cell Physiol. 2001 Jun;280(6):C1561-9. doi: 10.1152/ajpcell.2001.280.6.C1561. Am J Physiol Cell Physiol. 2001. PMID: 11350751 Free article.

10

Human-mouse differences in the embryonic expression patterns of developmental control genes and disease genes.

Fougerousse F, Bullen P, Herasse M, Lindsay S, Richard I, Wilson D, Suel L, Durand M, Robson S, Abitbol M, Beckmann JS, Strachan T. Fougerousse F, et al. Among authors: herasse m. Hum Mol Genet. 2000 Jan 22;9(2):165-73. doi: 10.1093/hmg/9.2.165. Hum Mol Genet. 2000. PMID: 10607827

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

Search Page

Search Results