Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 50 of 71

1.

GPs' management of polypharmacy and therapeutic dilemma in patients with multimorbidity: a cross-sectional survey of GPs in France.

Carrier H, Zaytseva A, Bocquier A, Villani P, Verdoux H, Fortin M, Verger P.

Br J Gen Pract. 2019 Feb 25. pii: bjgp19X701801. doi: 10.3399/bjgp19X701801. [Epub ahead of print]

PMID:
30803978
2.

Poor Health Literacy and Medication Burden Are Significant Predictors for Inadequate Bowel Preparation in an Urban Tertiary Care Setting.

Kunnackal John G, Thuluvath AJ, Carrier H, Ahuja NK, Gupta E, Stein E.

J Clin Gastroenterol. 2019 Feb 15. doi: 10.1097/MCG.0000000000001177. [Epub ahead of print]

PMID:
30789854
3.

Caring for patients with mental disorders in primary care: a qualitative study on French GPs' views, atittudes and needs.

Jego M, Debaty E, Ouirini L, Carrier H, Beetlestone E.

Fam Pract. 2019 Jan 25;36(1):72-76. doi: 10.1093/fampra/cmy107.

PMID:
30346525
4.

Effect of Automobile Travel Time Between Patients' Homes and Ophthalmologists' Offices on Screening for Diabetic Retinopathy.

Macon C, Carrier H, Janczewski A, Verger P, Casanova L.

Telemed J E Health. 2018 Jan;24(1):11-20. doi: 10.1089/tmj.2016.0271. Epub 2017 Jul 28.

PMID:
28753107
5.

[Trends in social inequities in diabetes care in the Provence-Alpes-Côte-d'Azur region of France between 2008 and 2011].

Casanova L, Carrier H, Martin de Vidales A, Cortaredona S, Verger P.

Rev Epidemiol Sante Publique. 2017 Feb;65(1):29-40. doi: 10.1016/j.respe.2016.10.060. Epub 2017 Jan 11. French.

PMID:
28089384
6.

Petroleomics by Direct Analysis in Real Time-Mass Spectrometry.

Romão W, Tose LV, Vaz BG, Sama SG, Lobinski R, Giusti P, Carrier H, Bouyssiere B.

J Am Soc Mass Spectrom. 2016 Jan;27(1):182-5. doi: 10.1007/s13361-015-1266-z. Epub 2015 Oct 2.

PMID:
26432579
7.

In vivo study of the kinematics in axial rotation of the lumbar spine after total intervertebral disc replacement: long-term results: a 10-14 years follow up evaluation.

SariAli el-H, Lemaire JP, Pascal-Mousselard H, Carrier H, Skalli W.

Eur Spine J. 2006 Oct;15(10):1501-10. Epub 2006 Jan 21.

PMID:
16429293
8.

Clinical and radiological outcomes with the Charité artificial disc: a 10-year minimum follow-up.

Lemaire JP, Carrier H, Sariali el-H, Skalli W, Lavaste F.

J Spinal Disord Tech. 2005 Aug;18(4):353-9. Erratum in: J Spinal Disord Tech. 2006 Feb;19(1):76. Sari Ali, El-Hadi [corrected to Sariali, El-hadi].

PMID:
16021017
9.

Overexpression of bcl-2 reduces sex differences in neuron number in the brain and spinal cord.

Zup SL, Carrier H, Waters EM, Tabor A, Bengston L, Rosen GJ, Simerly RB, Forger NG.

J Neurosci. 2003 Mar 15;23(6):2357-62.

10.

[Mitochondrial diabetes complicated by or associated with "MELAS" syndrome?].

Drouet A, Guilloton L, Godinot C, Rochet D, Ribot C, Carrier H.

Rev Neurol (Paris). 2000 Oct;156(10):892-5. French.

PMID:
11033519
11.

Immunolabelling of mitochondrial superoxide dismutase and of Hsp60 in muscles harbouring a respiratory chain deficiency.

Carrier H, Flocard F, Tagliati V, Arrigo AP, Godinot C.

Neuromuscul Disord. 2000 Feb;10(2):144-9.

PMID:
10714591
12.

[MELAS syndrome with pure vascular manifestation?].

Drouet A, Mousson B, Carrier H, Baverel G, Ribot C.

Rev Neurol (Paris). 1997 Oct;153(10):591-4. Review. French.

PMID:
9684024
13.

Selective neurotomy of the tibial nerve in the spastic hemiplegic child: an explanation of the recurrence.

Berard C, Sindou M, Berard J, Carrier H.

J Pediatr Orthop B. 1998 Jan;7(1):66-70.

PMID:
9481661
14.

Identification of a large-scale mitochondrial deoxyribonucleic acid deletion in endocrinopathies and deafness: report of two unrelated cases with diabetes mellitus and adrenal insufficiency, respectively.

Nicolino M, Ferlin T, Forest M, Godinot C, Carrier H, David M, Chatelain P, Mousson B.

J Clin Endocrinol Metab. 1997 Sep;82(9):3063-7.

PMID:
9284744
15.

Increase in oxidative key enzymes in a case of muscle ubiquinol-cytochrome c reductase deficiency.

Conjard A, Martin M, Ferrier B, Durozard D, Carrier H, Baverel G.

Acta Neuropathol. 1997 Jun;93(6):592-8.

PMID:
9194898
16.

[Dropped head syndrome: diagnostic discussion apropos of 3 cases].

Petiot P, Vial C, de Saint Victor JF, Charles N, Carrier H, Depierre P, Bady B.

Rev Neurol (Paris). 1997 May;153(4):251-5. Review. French.

PMID:
9296143
17.

Antimycin resistance and ubiquinol cytochrome c reductase instability associated with a human cytochrome b mutation.

Bouzidi MF, Carrier H, Godinot C.

Biochim Biophys Acta. 1996 Dec 16;1317(3):199-209.

18.

Variations of muscle mitochondrial creatine kinase activity in mitochondrial diseases.

Bouzidi MF, Enjolras N, Carrier H, Vial C, Lopez-Mediavilla C, Burt-Pichat B, Couthon F, Godinot C.

Biochim Biophys Acta. 1996 Jun 7;1316(2):61-70. Review.

19.

Molecular histology of mitochondrial and nuclear transcripts in the muscle of patients harbouring a single mitochondrial DNA deletion.

Carrier H, Burt-Pichat B, Flocard F, Guffon N, Mousson B, Dumoulin R, Godinot C.

Acta Neuropathol. 1996;91(1):104-11.

PMID:
8773154
20.

Effects of chronic renal failure on enzymes of energy metabolism in individual human muscle fibers.

Conjard A, Ferrier B, Martin M, Caillette A, Carrier H, Baverel G.

J Am Soc Nephrol. 1995 Jul;6(1):68-74.

21.

An abnormal exercise test response revealing a respiratory chain complex III deficiency.

Mousson B, Collombet JM, Dumoulin R, Carrier H, Flocard F, Bouzidi M, Godinot C, Maire I, Mathieu M, Quard S.

Acta Neurol Scand. 1995 Jun;91(6):488-93.

PMID:
7572045
22.

Fine mapping of randomly distributed multiple deletions of mitochondrial DNA in a case of chronic progressive external ophthalmoplegia.

Ville-Ferlin T, Dumoulin R, Stepien G, Matha V, Bady B, Flocard F, Carrier H, Mathieu M, Mousson B.

Mol Cell Probes. 1995 Jun;9(3):207-14.

PMID:
7477015
23.

Decreased expression of ubiquinol-cytochrome c reductase subunits in patients exhibiting mitochondrial myopathy with progressive exercise intolerance.

Bouzidi MF, Schägger H, Collombet JM, Carrier H, Flocard F, Quard S, Mousson B, Godinot C.

Neuromuscul Disord. 1993 Sep-Nov;3(5-6):599-604.

PMID:
8186719
24.

2-Ketoglutarate dehydrogenase deficiency, a rare cause of primary hyperlactataemia: report of a new case.

Guffon N, Lopez-Mediavilla C, Dumoulin R, Mousson B, Godinot C, Carrier H, Collombet JM, Divry P, Mathieu M, Guibaud P.

J Inherit Metab Dis. 1993;16(5):821-30.

PMID:
8295396
25.

Human cultured myoblasts: a model for the diagnosis of mitochondrial diseases.

Dumoulin R, Mandon G, Collombet JM, Blond JL, Carrier H, Godinot C, Flocard F, Villard J, Guibaud P, Mathieu M, et al.

J Inherit Metab Dis. 1993;16(3):545-7. No abstract available.

PMID:
7609448
26.

[Diagnosis of muscular intolerance during exercise caused by enzyme deficiency in adults].

Mousson B, Fléchaire A, Maire I, Flocard F, Van Uye A, Chaulet JF, Carrier H.

Rev Med Interne. 1992 Jan-Feb;13(1):43-8. French.

PMID:
1410874
27.

[Mitochondrial cytopathies].

Mousson B, Maire I, Carrier H, Flocard F, Flechaire A, Vidailhet M.

Rev Med Interne. 1991 May-Jun;12(3):219-26. Review. French.

PMID:
1896716
28.

Myopathic evolution of an exertional muscle pain syndrome with phosphorylase b kinase deficiency.

Carrier H, Maire I, Vial C, Rambaud G, Flocard F, Flechaire A.

Acta Neuropathol. 1990;81(1):84-8.

PMID:
2128163
29.

[Systematic neonatal detection of Duchenne's muscular dystrophy. Results after 10 years' of experience in Lyons (France)].

Plauchu H, Cordier MP, Carrier HN, Dellamonica C, Dorche C, Guibaud P, Lauras B, Cotte J, Robert JM.

J Genet Hum. 1987 Aug;35(4):217-30. French.

PMID:
3655748
30.

Congenital Lambert-Eaton myasthenic syndrome.

Bady B, Chauplannaz G, Carrier H.

J Neurol Neurosurg Psychiatry. 1987 Apr;50(4):476-8.

31.

[A case of myopathy with carnitine deficiency].

Martin P, Carrier H, Renaud JF, Kullmann B, Delpont E, Romey G, Cartier B, Bedoucha P.

Rev Neurol (Paris). 1986;142(6-7):625-34. French.

PMID:
3797933
32.

[Recurrent paroxysmal myoglobinuria with acute renal insufficiency caused by muscular carnitine (palmitoyltransferase deficiency. A case].

Meunier J, Perrot D, Bret M, Pissere-Meunier J, Bouletreau P, Pasquier J, Carrier H, Berthillier G.

Nouv Presse Med. 1982 Sep 25;11(37):2767-71. French.

PMID:
7145668
33.

Carnitine metabolism in early stages of Duchenne muscular dystrophy.

Berthillier G, Eichenberger D, Carrier HN, Guibaud P, Got R.

Clin Chim Acta. 1982 Jul 15;122(3):369-75.

PMID:
6125278
34.

Acute rhabdomyolysis with carnitine-palmityl-transferase deficiency.

Blanc PL, Carrier H, Thomas L, Chavaillon JM, Robert D.

Intensive Care Med. 1982;8(6):307. No abstract available.

PMID:
7175018
35.

[Psychosis treated with neuroleptics. Myositis and rise in serum creatine kinase during acute episodes].

Luaute JP, Zampa P, Forray JP, Brochier C, Carrier H, Guidollet J.

Nouv Presse Med. 1981 Sep 19;10(33):2751. French. No abstract available.

PMID:
6117053
36.

[Early clinical and histopathological manifestations in 14 boys showing elevated serum creatine-phosphokinase levels in their first year].

Guibaud P, Carrier HN, Plauchu H, Lauras B, Jolivet MJ, Robert JM.

J Genet Hum. 1981 Mar;29(1):71-84. French.

PMID:
7334343
37.

Carnitine levels in normal children and adults and in patients with diseases muscle.

Carrier HN, Berthillier G.

Muscle Nerve. 1980 Jul-Aug;3(4):326-34.

PMID:
7412776
38.

[Congenital myopathy with lipid and glycogen overload of muscle fiber and partial deficit of carnitine].

Gilly R, Carrier H, Lamit J.

Ann Pediatr (Paris). 1980 May;27(5):319-24. French. No abstract available.

PMID:
6940512
39.

[Hypotonia and convulsive encephalopathy with lipid myopathy and palmitoyl-carnitine transferase deficiency. A new entity?].

Hermier M, Carrier H, Berthillier G, Feit JP, Jeune M.

Pediatrie. 1979 Jul-Aug;34(5):503-18. French. No abstract available.

PMID:
503721
40.

[Oculocraniosomatic neuromuscular disease].

Feit JP, Carrier H, David M, Macabéo V, Vibert J, Mathieu M, Jeune M.

Arch Fr Pediatr. 1979 May;36(5):487-92. French.

PMID:
496542
41.

[Lipidic myopathy with severe cardiomyopathy caused by a generalized carnitine deficiency. Favourable course during carnitine hydrochloride treatment].

Morand P, Despert F, Carrier HN, Saudubray BM, Fardeau M, Romieux B, Fauchier C, Combe P.

Arch Mal Coeur Vaiss. 1979 May;72(5):536-44. French.

PMID:
115407
42.

[Primary cardiomyopathy in children with lipid infiltration of the myocardium and skeletal muscles and demonstration of a palmityl-carnitine transferase deficiency. Apropos of 4 cases].

Normand J, Carrier H, Berthillier G, Bozio A, Jocteur-Monrozier D, André M, Joffre B.

Arch Mal Coeur Vaiss. 1979 May;72(5):529-35. French.

PMID:
115406
43.

[Familial congenital muscular dystrophy caused by phosphofructokinase deficiency].

Guibaud P, Carrier H, Mathieu M, Dorche C, Parchoux B, Béthenod M, Larbre F.

Arch Fr Pediatr. 1978 Dec;35(10):1105-15. French.

PMID:
155429
44.
45.

[Heterogeneity of glycogenosis with alpha-1,4-glucosidase deficiency: enzymatic studies in three families (author's transl)].

Bienvenu J, Carrier H, Freycon F, Mathieu M.

Clin Chim Acta. 1978 Mar 15;84(3):277-92. French.

PMID:
346265
46.

[Toxic neurologic manifestations during angina pectoris treatment (perhexiline maleate and amiotadone hydrochloride)].

Bady B, Bourrat C, Trillet M, Girard PF, Carrier H.

Int J Neurol. 1978;11(4):371-82. Review. French. No abstract available.

PMID:
232499
47.

[Hemispheric asymmetries of the human brain].

Kopp N, Michel F, Carrier H, Biron A, Duvillard P.

J Neurol Sci. 1977 Dec;34(3):349-63. French.

PMID:
591994
48.

[Use of local cobalt therapy in peripheral neuropathies associated with chronic lymphopathies (lymphoses). 2 cases with histo-immunologic and ultrastructural records].

Masson R, Carrier H, Barbaret C, Boucher M, Chazot G, Peaud PY, Revol L.

Rev Neurol (Paris). 1977 Aug-Sep;133(8-9):475-84. French.

PMID:
412243
49.

[Proliferation of the transverse tubular system during a tardive and familial myopathy].

Carrier H, Tommasi M, Kopp N, Boisson D.

J Neurol Sci. 1976 Apr;27(4):499-512. French.

PMID:
1262907
50.

[Neurological manifestations in monoclonal gammapathies. Pure neurological manifestations. Immunofluorescence study].

Chazot G, Berger B, Carrier H, Barbaret C, Bady B, Dumas R, Creyssel R, Schott B.

Rev Neurol (Paris). 1976 Mar;132(3):195-212. French.

PMID:
184514

Supplemental Content

Loading ...
Support Center