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Papers authored by Verny C

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OPA1-associated disorders: phenotypes and pathophysiology.

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Amati-Bonneau P, Milea D, Bonneau D, Chevrollier A, Ferré M, Guillet V, Gueguen N, Loiseau D, de Crescenzo MA, Verny C, Procaccio V, Lenaers G, and Reynier P

The international journal of biochemistry & cell biology 41(10):1855-65, 2009 Oct - Who cited this? | PubMed ID: 19389487 | Fulltext

A genetic variation in the ADORA2A gene modifies age at onset in Huntington's disease.

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Dhaenens CM, Burnouf S, Simonin C, Van Brussel E, Duhamel A, Defebvre L, Duru C, Vuillaume I, Cazeneuve C, Charles P, Maison P, Debruxelles S, Verny C, Gervais H, Azulay JP, Tranchant C,

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Neurobiology of disease 35(3):474-6, 2009 Sep - Who cited this? | PubMed ID: 19591938 | Fulltext

Key priorities in managing glucose control in older people with diabetes.

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Bourdel Marchasson I, Doucet J, Bauduceau B, Berrut G, Blickle JF, Brocker P, Constans T, Fagot Campagna A, Kaloustian E, Lassmann Vague V, Lecomte P, Simon D, Tessier D, Verny C, and Vischer UM

The journal of nutrition, health & aging 13(8):685-91, 2009 Aug - Who cited this? | PubMed ID: 19657551 | Fulltext

In vivo evidence for the selective subcortical degeneration in Huntington's disease.

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Douaud G, Behrens TE, Poupon C, Cointepas Y, Jbabdi S, Gaura V, Golestani N, Krystkowiak P, Verny C, Damier P, Bachoud-Lévi AC, Hantraye P, and Remy P

NeuroImage 46(4):958-66, 2009 Jul 15 - Who cited this? | PubMed ID: 19332141 | Fulltext

Molecular screening of 980 cases of suspected hereditary optic neuropathy with a report on 77 novel OPA1 mutations.

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Ferré M, Bonneau D, Milea D, Chevrollier A, Verny C, Dollfus H, Ayuso C, Defoort S, Vignal C, Zanlonghi X, Charlin JF, Kaplan J, Odent S, Hamel CP, Procaccio V, Reynier P,

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Human mutation 30(7):E692-705, 2009 Jul - Who cited this? | PubMed ID: 19319978 | Fulltext

A call to incorporate the prevention and treatment of geriatric disorders in the management of diabetes in the elderly.

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Vischer UM, Bauduceau B, Bourdel-Marchasson I, Blickle JF, Constans T, Fagot-Campagna A, Kaloustian E, Lassman-Vague V, Lecomte P, Simon D, Tessier D, Verny C, Doucet J, and Alfediam/SFGG French-speaking group for study of diabetes in the elderly

Diabetes & metabolism 35(3):168-77, 2009 Jun - Who cited this? | PubMed ID: 19446486 | Fulltext

Mitochondrial complex I deficiency in GDAP1-related autosomal dominant Charcot-Marie-Tooth disease (CMT2K).

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Cassereau J, Chevrollier A, Gueguen N, Malinge MC, Letournel F, Nicolas G, Richard L, Ferre M, Verny C, Dubas F, Procaccio V, Amati-Bonneau P, Bonneau D, and Reynier P

Neurogenetics 10(2):145-50, 2009 Apr - Who cited this? | PubMed ID: 19089472 | Fulltext

[In Process Citation].

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Verny C, Gonzalez B, Lanfranchi G, and Hervy MP

Soins. Gerontologie(76):18-21, 2009 - Who cited this? | PubMed ID: 19366019 | Fulltext

Mitochondrial DNA A3243G mutation involved in familial diabetes, chronic intestinal pseudo-obstruction and recurrent pancreatitis.

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Verny C, Amati-Bonneau P, Letournel F, Person B, Dib N, Malinge MC, Slama A, Le Maréchal C, Ferec C, Procaccio V, Reynier P, and Bonneau D

Diabetes & metabolism 34(6):620-6, 2008 Dec - Who cited this? | PubMed ID: 18955007 | Fulltext

Hereditary amyloid neuropathy by transthyretin Val107 mutation in a patient of African origin.

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Cassereau J, Lavigne C, Letournel F, Ghali A, Verny C, Dubas F, Devière F, and Nicolas G

Journal of the peripheral nervous system : JPNS 13(3):251-4, 2008 Sep - Who cited this? | PubMed ID: 18844793 | Fulltext

Hereditary optic neuropathies share a common mitochondrial coupling defect.

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Chevrollier A, Guillet V, Loiseau D, Gueguen N, de Crescenzo MA, Verny C, Eng MF, Dollfus H, Odent S, Milea D, Goizet C, Amati-Bonneau P, Procaccio V, Bonneau D, and Reynier P

Annals of neurology 63(6):794-8, 2008 Jun - Who cited this? | PubMed ID: 18496845 | Fulltext

Language processing within the striatum: evidence from a PET correlation study in Huntington's disease.

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Teichmann M, Gaura V, Démonet JF, Supiot F, Delliaux M, Verny C, Renou P, Remy P, and Bachoud-Lévi AC

Brain : a journal of neurology 131(Pt 4):1046-56, 2008 Apr - Who cited this? | PubMed ID: 18334537 | Fulltext

Multiple sclerosis-like disorder in opa1-related autosomal dominant optic atrophy.

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Verny C, Loiseau D, Scherer C, Lejeune P, Chevrollier A, Gueguen N, Guillet V, Dubas F, Reynier P, Amati-Bonneau P, and Bonneau D

Neurology 70(13 Pt 2):1152-3, 2008 Mar 25 - Who cited this? | PubMed ID: 18287570 | Fulltext

Heterozygosity for a single mutation in the ABCC6 gene may closely mimic PXE: consequences of this phenotype overlap for the definition of PXE.

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Martin L, Maître F, Bonicel P, Daudon P, Verny C, Bonneau D, Le Saux O, and Chassaing N

Archives of dermatology 144(3):301-6, 2008 Mar - Who cited this? | PubMed ID: 18347285 | Fulltext

OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes.

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Amati-Bonneau P, Valentino ML, Reynier P, Gallardo ME, Bornstein B, Boissière A, Campos Y, Rivera H, de la Aleja JG, Carroccia R, Iommarini L, Labauge P, Figarella-Branger D, Marcorelles P, Furby A, Beauvais K,

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Brain : a journal of neurology 131(Pt 2):338, 2008 Feb - Who cited this? | PubMed ID: 18158317 | Fulltext

Middle cerebral artery dissection gives rise to giant serpentine aneurysm.

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Verny C, Marc G, Pasco A, and Dubas F

Cerebrovascular diseases (Basel, Switzerland) 25(3):283-5, 2008 - Who cited this? | PubMed ID: 18332625 | Fulltext

Cognitive changes in asymptomatic carriers of the Huntington disease mutation gene.

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Verny C, Allain P, Prudean A, Malinge MC, Gohier B, Scherer C, Bonneau D, Dubas F, and Le Gall D

European journal of neurology : the official journal of the European Federation of Neurological Societies 14(12):1344-50, 2007 Dec - Who cited this? | PubMed ID: 17941857 | Fulltext

Mitochondrial coupling defect in Charcot-Marie-Tooth type 2A disease.

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Loiseau D, Chevrollier A, Verny C, Guillet V, Gueguen N, Pou de Crescenzo MA, Ferré M, Malinge MC, Guichet A, Nicolas G, Amati-Bonneau P, Malthièry Y, Bonneau D, and Reynier P

Annals of neurology 61(4):315-23, 2007 Apr - Who cited this? | PubMed ID: 17444508 | Fulltext

Congestive heart failure in the elderly diabetic.

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Verny C

Diabetes & metabolism 33 Suppl 1:S32-9, 2007 Apr - Who cited this? | PubMed ID: 17702097 | Fulltext

Phenotype associated with APP duplication in five families.

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Cabrejo L, Guyant-Maréchal L, Laquerrière A, Vercelletto M, De la Fournière F, Thomas-Antérion C, Verny C, Letournel F, Pasquier F, Vital A, Checler F, Frebourg T, Campion D, and Hannequin D

Brain : a journal of neurology 129(Pt 11):2966, 2006 Nov - Who cited this? | PubMed ID: 16959815 | Fulltext

Refsum's disease may mimic familial Guillain Barre syndrome.

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Verny C, Prundean A, Nicolas G, Pautot V, Maugin D, Levade T, Bonneau D, and Dubas F

Neuromuscular disorders : NMD 16(11):805-8, 2006 Nov - Who cited this? | PubMed ID: 16934464 | Fulltext

Distribution of grey matter atrophy in Huntington's disease patients: a combined ROI-based and voxel-based morphometric study.

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Douaud G, Gaura V, Ribeiro MJ, Lethimonnier F, Maroy R, Verny C, Krystkowiak P, Damier P, Bachoud-Levi AC, Hantraye P, and Remy P

NeuroImage 32(4):1562-75, 2006 Oct 1 - Who cited this? | PubMed ID: 16875847 | Fulltext

[Idiopathic acute transverse myelitis: application of new diagnosis criteria to 17 patients].

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Lanctin C, Wiertlewski S, Moreau C, Verny C, Derkinderen P, Damier P, and Dubas F

Revue neurologique 162(10):980-9, 2006 Oct - Who cited this? | PubMed ID: 17028566 | Fulltext

Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutations.

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Azzedine H, Ravisé N, Verny C, Gabrëels-Festen A, Lammens M, Grid D, Vallat JM, Durosier G, Senderek J, Nouioua S, Hamadouche T, Bouhouche A, Guilbot A, Stendel C, Ruberg M, Brice A,

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Neurology 67(4):602-6, 2006 Aug 22 - Who cited this? | PubMed ID: 16924012 | Fulltext

Autosomal-recessive forms of demyelinating Charcot-Marie-Tooth disease.

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Dubourg O, Azzedine H, Verny C, Durosier G, Birouk N, Gouider R, Salih M, Bouhouche A, Thiam A, Grid D, Mayer M, Ruberg M, Tazir M, Brice A, and LeGuern E

Neuromolecular medicine 8(1-2):75-86, 2006 - Who cited this? | PubMed ID: 16775368 | Fulltext

OPA1 R445H mutation in optic atrophy associated with sensorineural deafness.

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Amati-Bonneau P, Guichet A, Olichon A, Chevrollier A, Viala F, Miot S, Ayuso C, Odent S, Arrouet C, Verny C, Calmels MN, Simard G, Belenguer P, Wang J, Puel JL, Hamel C,

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Annals of neurology 58(6):958-63, 2005 Dec - Who cited this? | PubMed ID: 16240368 | Fulltext

Management of dyslipidemia in elderly diabetic patients.

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Verny C

Diabetes & metabolism 31 Spec No 2:5S74-5S81, 2005 Dec - Who cited this? | PubMed ID: 16415769 | Fulltext

[Diabetes in the aged].

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Verny C

Soins; la revue de reference infirmiere(694 Pt 2):27-9, 2005 Apr - Who cited this? | PubMed ID: 15869247 | Fulltext

[An OPA3 gene mutation is responsible for the disease associating optic atrophy and cataract with extrapyramidal signs].

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Verny C, Amati-Bonneau P, Dubas F, Malthiéry Y, Reynier P, and Bonneau D

Revue neurologique 161(4):451-4, 2005 Apr - Who cited this? | PubMed ID: 15924081 | Fulltext

Arithmetic word-problem-solving in Huntington's disease.

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Allain P, Verny C, Aubin G, Pinon K, Bonneau D, Dubas F, and Le Gall D

Brain and cognition 57(1):1-3, 2005 Feb - Who cited this? | PubMed ID: 15629205 | Fulltext

Isolated Horner's syndrome may herald stroke.

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de Bray JM, Baumgartner R, Guillon B, Pautot V, Dziewas R, Ringelstein EB, Sturzenegger M, Garnier P, Ducrocq X, Saudeau D, Neau JP, Larrue V, Vuillier F, Boulliat J, Verret JM, Verny C,

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Cerebrovascular diseases (Basel, Switzerland) 19(4):274-5, 2005 - Who cited this? | PubMed ID: 15761221 | Fulltext

Coincidence of two genetic forms of Charcot-Marie-Tooth disease in a single family.

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Verny C, Ravisé N, Leutenegger AL, Pouplard F, Dubourg O, Tardieu S, Dubas F, Brice A, Genin E, and LeGuern E

Neurology 63(8):1527-9, 2004 Oct 26 - Who cited this? | PubMed ID: 15505184 | Fulltext

[Genetics of specific language impairments].

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Bonneau D, Verny C, and Uzé J

Archives de pediatrie : organe officiel de la Societe francaise de pediatrie 11(10):1213-6, 2004 Oct - Who cited this? | PubMed ID: 15475279 | Fulltext

OPA3 gene mutations responsible for autosomal dominant optic atrophy and cataract.

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Reynier P, Amati-Bonneau P, Verny C, Olichon A, Simard G, Guichet A, Bonnemains C, Malecaze F, Malinge MC, Pelletier JB, Calvas P, Dollfus H, Belenguer P, Malthièry Y, Lenaers G, and Bonneau D

Journal of medical genetics 41(9):e110, 2004 Sep - Who cited this? | PubMed ID: 15342707 | Fulltext

[Processing of "scripts" and frontal lobe function in Huntington's disease].

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Allain P, Verny C, Aubin G, Bonneau D, Dubas F, and Le Gall D

Revue neurologique 160(4 Pt 1):434-40, 2004 Apr - Who cited this? | PubMed ID: 15103268 | Fulltext

Chfr inactivation is not associated to chromosomal instability in colon cancers.

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Bertholon J, Wang Q, Falette N, Verny C, Auclair J, Chassot C, Navarro C, Saurin JC, and Puisieux A

Oncogene 22(55):8956-60, 2003 Dec 4 - Who cited this? | PubMed ID: 14654793 | Fulltext

Estimation of the inbreeding coefficient through use of genomic data.

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Leutenegger AL, Prum B, Génin E, Verny C, Lemainque A, Clerget-Darpoux F, and Thompson EA

American journal of human genetics 73(3):516-23, 2003 Sep - Who cited this? | PubMed ID: 12900793 | Fulltext

Two clinicopathological cases of a dominantly inherited, adult onset orthochromatic leucodystrophy.

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Letournel F, Etcharry-Bouyx F, Verny C, Barthelaix A, and Dubas F

Journal of neurology, neurosurgery, and psychiatry 74(5):671-3, 2003 May - Who cited this? | PubMed ID: 12700318 | Fulltext

A mutation in periaxin is responsible for CMT4F, an autosomal recessive form of Charcot-Marie-Tooth disease.

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Guilbot A, Williams A, Ravisé N, Verny C, Brice A, Sherman DL, Brophy PJ, LeGuern E, Delague V, Bareil C, Mégarbané A, and Claustres M

Human molecular genetics 10(4):415-21, 2001 Feb 15 - Who cited this? | PubMed ID: 11157804 | Fulltext

Molecular epidemiology of an outbreak due to IRT-2 beta-lactamase-producing strains of Klebsiella pneumoniae in a geriatric department.

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Girlich D, Karim A, Poirel L, Cavin MH, Verny C, and Nordmann P

The Journal of antimicrobial chemotherapy 45(4):467-73, 2000 Apr - Who cited this? | PubMed ID: 10747823 | Fulltext

[Spontaneous spinal cord herniation: a little-known cause of Brown-Sequard syndrome. Report of two cases and review of the literature].

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Verny C, Mercier P, Hayek G, Fournier D, Menei P, and Guy G

Neuro-Chirurgie 45(3):225-31, 1999 Sep - Who cited this? | PubMed ID: 10567963 | Fulltext

[Diabetes in the elderly].

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Blickle JF, Attali JR, Barrou Z, Brocker P, De Rekeneire N, Verny C, and Leutenegger M

Diabetes & metabolism 25(1):84-93, 1999 Mar - Who cited this? | PubMed ID: 10335428 | Fulltext

Association between intra-abdominal fat and hypertension in android obese diabetics.

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Sepulveda-Lavados A, Bastard JP, Attal M, Belin MF, Sachon C, Verny C, and Grimaldi A

Annales de medecine interne 147(6):393-16, 1996 - Who cited this? | PubMed ID: 9092341 | Fulltext

[Nocturnal hypoglycemia in insulin-dependent diabetics].

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Verny C, Remy C, Sachon C, Bosquet F, Casanova S, and Grimaldi A

Presse medicale (Paris, France : 1983) 24(26):1198-200, 1995 Sep 16 - Who cited this? | PubMed ID: 7567846 | Fulltext

[Non-perception of hypoglycemia].

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Grimaldi A, Sachon C, Bosquet F, Verny C, Barrou B, and Bitker MO

Journees annuelles de diabetologie de l'Hotel-Dieu:223-39, 1994 - Who cited this? | PubMed ID: 8051824 | Fulltext

[Hospitalization in internal medicine of nonagenarians. Study of 150 cases].

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Saint Jean O, Thibert JB, Holstein J, Bourdiol MC, Verny M, Berigaud S, Verny C, and Bouchon JP

La Revue de medecine interne / fondee ... par la Societe nationale francaise de medecine interne 14(9):825-31, 1993 - Who cited this? | PubMed ID: 8191100 | Fulltext

[Nephropathy caused by iodinated contrast media and diabetes].

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Permal S, Verny C, Bellin MF, Grellet J, and Grimaldi A

Journal de radiologie 73(2):79-81, 1992 Feb - Who cited this? | PubMed ID: 1602442 | Fulltext

[Heart conduction disorders in long-term treatment with chloroquine. Two new cases].

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Verny C, de Gennes C, Sébastien P, Lê Thi HD, Chapelon C, Piette JC, Chomette G, and Godeau P

Presse medicale (Paris, France : 1983) 21(17):800-4, 1992 - Who cited this? | PubMed ID: 1535141 | Fulltext

[Lipoprotein A].

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Verny C and Faucher C

Annales de medecine interne 143(3):184-90, 1992 - Who cited this? | PubMed ID: 1524352 | Fulltext

[Nephropathy caused by iodinated contrast media and diabetes mellitus].

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Permal S, Verny C, Bellin MF, Grellet J, and Grimaldi A

Journal d'urologie 98(1):46-9, 1992 - Who cited this? | PubMed ID: 1527399 | Fulltext

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