A Ducros

Summary

Country: France

Publications

  1. ncbi request reprint [Thunderclap headache]
    A Ducros
    Centre d Urgences Céphalées, Hopital Lariboisiere, Paris, France
    Rev Neurol (Paris) 161:713-5. 2005
  2. ncbi request reprint [Cluster headache]
    Anne Ducros
    Centre d Urgences Céphalées, Hopital Lariboisiere, Ambroise Paré, Paris
    Ann Med Interne (Paris) 154:468-74. 2003
  3. ncbi request reprint The genetics of migraine
    Anne Ducros
    Headache Emergency Department, Lariboisiere Hospital, Paris, France
    Lancet Neurol 1:285-93. 2002
  4. ncbi request reprint [Mechanisms and genetics of migraine]
    Anne Ducros
    Centre d Urgences Céphalées, Hôpital Lariboisère, Paris, France
    CNS Drugs 20:1-11. 2006
  5. ncbi request reprint The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel
    A Ducros
    INSERM E99 21, Faculté de Médecine Lariboisiere, Paris, France
    N Engl J Med 345:17-24. 2001
  6. ncbi request reprint Skin biopsy immunostaining with a Notch3 monoclonal antibody for CADASIL diagnosis
    A Joutel
    INSERM EPI 99 21, Faculté de Médecine Lariboisiere, 10 Avenue de Verdun, 75010, Paris, France
    Lancet 358:2049-51. 2001
  7. ncbi request reprint A human homolog of bacterial acetolactate synthase genes maps within the CADASIL critical region
    A Joutel
    INSERM U25, Paris, France
    Genomics 38:192-8. 1996
  8. ncbi request reprint Missense CACNA1A mutation causing episodic ataxia type 2
    C Denier
    INSERM EPI 99 21, Faculté de Médecine Lariboisiere, 10, avenue de Verdun, 75010 Paris, France
    Arch Neurol 58:292-5. 2001
  9. doi request reprint De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraine
    F Riant
    Laboratoire de Genetique Moleculaire, APHP Hôpital Lariboisière, Paris, France
    Neurology 75:967-72. 2010
  10. ncbi request reprint CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophy
    K Vahedi
    Service de Neurologie, Hopital Lariboisiere, Paris, France
    Neurology 55:1040-2. 2000

Collaborators

Detail Information

Publications23

  1. ncbi request reprint [Thunderclap headache]
    A Ducros
    Centre d Urgences Céphalées, Hopital Lariboisiere, Paris, France
    Rev Neurol (Paris) 161:713-5. 2005
    ..The search for a cause should be expedient and exhaustive. In the absence of an identified cause, the international headache classification suggests to consider the diagnosis of primary thunderclap headache, which remains controversial...
  2. ncbi request reprint [Cluster headache]
    Anne Ducros
    Centre d Urgences Céphalées, Hopital Lariboisiere, Ambroise Paré, Paris
    Ann Med Interne (Paris) 154:468-74. 2003
    ..Prophylactic treatment is often needed to reduce the daily frequency of attacks: verapamil in episodic cluster headache and lithium in chronic cluster headache...
  3. ncbi request reprint The genetics of migraine
    Anne Ducros
    Headache Emergency Department, Lariboisiere Hospital, Paris, France
    Lancet Neurol 1:285-93. 2002
    ..Another locus for migraine may be on the X chromosome. Finally, many positive association studies have been published, but few have been replicated...
  4. ncbi request reprint [Mechanisms and genetics of migraine]
    Anne Ducros
    Centre d Urgences Céphalées, Hôpital Lariboisère, Paris, France
    CNS Drugs 20:1-11. 2006
    ..Trigeminovascular fibres transmit nociceptive information centrally via the brainstem. The trigeminovascular fibres also activate the parasympathetic system that is responsible for the persistence of vasodilation in meningeal vessels...
  5. ncbi request reprint The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel
    A Ducros
    INSERM E99 21, Faculté de Médecine Lariboisiere, Paris, France
    N Engl J Med 345:17-24. 2001
    ..We studied the various clinical manifestations associated with mutations in CACNA1A in families with hemiplegic migraine with and without cerebellar signs...
  6. ncbi request reprint Skin biopsy immunostaining with a Notch3 monoclonal antibody for CADASIL diagnosis
    A Joutel
    INSERM EPI 99 21, Faculté de Médecine Lariboisiere, 10 Avenue de Verdun, 75010, Paris, France
    Lancet 358:2049-51. 2001
    ..Our immunostaining technique is highly sensitive (96%) and specific (100%) for diagnosis of CADASIL...
  7. ncbi request reprint A human homolog of bacterial acetolactate synthase genes maps within the CADASIL critical region
    A Joutel
    INSERM U25, Paris, France
    Genomics 38:192-8. 1996
    ....
  8. ncbi request reprint Missense CACNA1A mutation causing episodic ataxia type 2
    C Denier
    INSERM EPI 99 21, Faculté de Médecine Lariboisiere, 10, avenue de Verdun, 75010 Paris, France
    Arch Neurol 58:292-5. 2001
    ..To characterize the nature of CACNA1A mutation in a previously unreported family with episodic ataxia type 2 (EA2) and to better delineate EA2 clinical features...
  9. doi request reprint De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraine
    F Riant
    Laboratoire de Genetique Moleculaire, APHP Hôpital Lariboisière, Paris, France
    Neurology 75:967-72. 2010
    ..Screening of FHM genes in previous series of patients with SHM detected a very low proportion of mutated patients. In this study, we investigated the FHM genes in patients with an early onset sporadic form of HM (onset before 16 years)...
  10. ncbi request reprint CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophy
    K Vahedi
    Service de Neurologie, Hopital Lariboisiere, Paris, France
    Neurology 55:1040-2. 2000
    ..This patient carried a de novo Tyr 1385 Cys mutation in the CACNA1A gene and illustrates a novel phenotype associated with CACNA1A mutations...
  11. ncbi request reprint Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneity
    A Ducros
    INSERM U25, Faculte de Medecine Necker, Hopital Lariboisiere, Paris, France
    Ann Neurol 42:885-90. 1997
    ..Chromosome 1-linked families differ from the ones linked to chromosome 19, because penetrance in those families is much lower, and in some of their members, epileptic seizures occur during severe migraine attacks...
  12. ncbi request reprint Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia
    A Joutel
    INSERM U25, Faculte de Medecine Necker Enfants Malades, Paris, France
    Nature 383:707-10. 1996
    ..We have identified mutations in CADASIL patients that cause serious disruption of this gene, indicating that Notch3 could be the defective protein in CADASIL patients...
  13. ncbi request reprint [Akinetic mutism and anterior bicerebral infarction due to abnormal distribution of the anterior cerebral artery]
    V Wolff
    Service de Neurologie, Hopital Lariboisiere, Paris, France
    Rev Neurol (Paris) 158:377-80. 2002
  14. ncbi request reprint Chronic paroxysmal hemicrania in a patient with a macroprolactinoma
    M Sarov
    Emergency Headache Centre, Lariboisiere Hospital, Paris, France
    Cephalalgia 26:738-41. 2006
    ..Investigations revealed a macroprolactinoma. Headaches stopped after cabergoline treatment. This report further suggests that patients with paroxysmal hemicrania should be investigated for pituitary abnormalities...
  15. doi request reprint [Reversible cerebral vasoconstriction syndrome]
    A Ducros
    Pôle Neurosensoriel, Centre d Urgences Céphalées, Hopital Lariboisiere, AP HP, 2 rue Ambroise Pare, 75475 Paris Cedex 10, France
    Rev Neurol (Paris) 166:365-76. 2010
    ..Relapses are possible but rare and have not been reported yet in prospective series. It seems appropriate to advise the patients to avoid sympathomimetic and serotoninergic substances...
  16. doi request reprint Emergency treatment of migraine
    A Ducros
    Centre d Urgences Céphalées, Hopital Lariboisiere, Paris, France
    Cephalalgia 28:9-13. 2008
    ....
  17. ncbi request reprint Early epidural blood patch in spontaneous intracranial hypotension
    S Berroir
    Service de Neurologie, Lariboisiere Hospital, Paris, France
    Neurology 63:1950-1. 2004
    ..Spontaneous intracranial hypotension with typical orthostatic headache can be diagnosed without lumbar puncture and can be cured by early EBP in a majority of patients...
  18. ncbi request reprint Late-onset eosinophilic chronic meningitis occurring 30 years after Taenia solium infestation in a white Caucasian woman
    H Castillo-Iglesias
    Department of Internal Medicine, Lariboisiere Hospital, AP HP, 75010 Paris, France
    J Infect 53:e35-8. 2006
    ..The patient showed considerable improvement following treatment with albendazole and prednisone...
  19. ncbi request reprint Familial cluster headache: a series of 186 index patients
    Mohammed El Amrani
    Service de Neurologie, Clinique de Courlancy, Reims, France
    Headache 42:974-7. 2002
    ..To investigate the familial occurrence of cluster headache in a series of French patients fulfilling the International Headache Society diagnosis criteria...
  20. ncbi request reprint Most cases labeled as "retinal migraine" are not migraine
    Donna L Hill
    Departments of Ophthalmology, Emory University School of Medicine, Atlanta, Georgia, USA
    J Neuroophthalmol 27:3-8. 2007
    ....
  21. ncbi request reprint [Acute and chronic headaches]
    Anne Ducros
    Urgences Cephalees, Hopital Lariboisiere, 75010 Paris
    Rev Prat 56:2161-72. 2006
  22. ncbi request reprint ATP1A2 mutations in 11 families with familial hemiplegic migraine
    Florence Riant
    Laboratoire de Genetique Moleculaire, Hôpital Lariboisière AP HP, Paris, France
    Hum Mutat 26:281. 2005
    ..Genotyping of 94 relatives of these 11 probands identified 47 mutation carriers, among whom 36 were clinically affected. Sequencing of all 23 exons in an ethnically matched panel detected only one exonic coding polymorphism...
  23. ncbi request reprint A negative D-dimer assay does not rule out cerebral venous thrombosis: a series of seventy-three patients
    Isabelle Crassard
    Neurology Department, Lariboisiere Hospital, 2 rue Ambroise Pare, 75010 Paris, France
    Stroke 36:1716-9. 2005
    ..Previous reports have emphasized the potential clinical utility of D-dimer assay in CVT diagnosis...