Galmiche L - Search Results

1

Normal oxidative phosphorylation in intestinal smooth muscle of childhood chronic intestinal pseudo-obstruction.

Galmiche L, Jaubert F, Sauvat F, Sarnacki S, Goulet O, Assouline Z, Vedrenne V, Lebre AS, Boddaert N, Brousse N, Chrétien D, Munnich A, Rötig A. Galmiche L, et al. Neurogastroenterol Motil. 2011 Jan;23(1):24-9, e1. doi: 10.1111/j.1365-2982.2010.01595.x. Epub 2010 Sep 14. Neurogastroenterol Motil. 2011. PMID: 20879992

2

[Lynch syndrome pediatric: about a case].

Galmiche L, Révillon Y, Sarnacki S, Jaubert F. Galmiche L, et al. Ann Pathol. 2004 Dec;24(6):621-3. doi: 10.1016/s0242-6498(04)94023-0. Ann Pathol. 2004. PMID: 15785407 French.

3

Development of liver disease despite mannose treatment in two patients with CDG-Ib.

Mention K, Lacaille F, Valayannopoulos V, Romano S, Kuster A, Cretz M, Zaidan H, Galmiche L, Jaubert F, de Keyzer Y, Seta N, de Lonlay P. Mention K, et al. Among authors: galmiche l. Mol Genet Metab. 2008 Jan;93(1):40-3. doi: 10.1016/j.ymgme.2007.08.126. Epub 2007 Oct 22. Mol Genet Metab. 2008. PMID: 17945525

4

[Diagnosis of renal metanephric adenoma: relevance of immunohistochemistry and biopsy].

Galmiche L, Vasiliu V, Poirée S, Hélénon O, Casanova JM, Brousse N. Galmiche L, et al. Ann Pathol. 2007 Oct;27(5):365-8. doi: 10.1016/s0242-6498(07)78275-5. Ann Pathol. 2007. PMID: 18185471 French.

5

Diffuse lymphoplasmacytic bronchiolitis in cartilage-hair hypoplasia.

Bailly-Botuha C, Jaubert F, Taam RA, Galmiche L, Picard C, Bellon G, de Blic J. Bailly-Botuha C, et al. Among authors: galmiche l. J Pediatr. 2008 Mar;152(3):429-33. doi: 10.1016/j.jpeds.2007.10.010. J Pediatr. 2008. PMID: 18280854

6

Transcription factors involved in pancreas development are expressed in paediatric solid pseudopapillary tumours.

Galmiche L, Sarnacki S, Verkarre V, Boizet B, Duvillie B, Fabre M, Jaubert F. Galmiche L, et al. Histopathology. 2008 Sep;53(3):318-24. doi: 10.1111/j.1365-2559.2008.03108.x. Epub 2008 Jul 29. Histopathology. 2008. PMID: 18671802

7

Mutation in the mitochondrial translation elongation factor EFTs results in severe infantile liver failure.

Vedrenne V, Galmiche L, Chretien D, de Lonlay P, Munnich A, Rötig A. Vedrenne V, et al. Among authors: galmiche l. J Hepatol. 2012 Jan;56(1):294-7. doi: 10.1016/j.jhep.2011.06.014. Epub 2011 Jul 8. J Hepatol. 2012. PMID: 21741925 Free article.

8

Exome sequencing identifies MRPL3 mutation in mitochondrial cardiomyopathy.

Galmiche L, Serre V, Beinat M, Assouline Z, Lebre AS, Chretien D, Nietschke P, Benes V, Boddaert N, Sidi D, Brunelle F, Rio M, Munnich A, Rötig A. Galmiche L, et al. Hum Mutat. 2011 Nov;32(11):1225-31. doi: 10.1002/humu.21562. Epub 2011 Sep 14. Hum Mutat. 2011. PMID: 21786366

9

Toward genotype phenotype correlations in GFM1 mutations.

Galmiche L, Serre V, Beinat M, Zossou R, Assouline Z, Lebre AS, Chretien F, Shenhav R, Zeharia A, Saada A, Vedrenne V, Boddaert N, de Lonlay P, Rio M, Munnich A, Rötig A. Galmiche L, et al. Mitochondrion. 2012 Mar;12(2):242-7. doi: 10.1016/j.mito.2011.09.007. Epub 2011 Oct 1. Mitochondrion. 2012. PMID: 21986555

10

Foxl-2 in gonad development and pathology.

Jaubert F, Galmiche L, Lortat-Jacob S, Fournet JC, Fellous M. Jaubert F, et al. Among authors: galmiche l. Arkh Patol. 2011 Jul-Aug;73(4):10-3. Arkh Patol. 2011. PMID: 22164424 Review.

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