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21 results on '"Hohl D"'

1. Congenital ichthyoses: European guidelines of care, part two

Author

Mazereeuw‐Hautier, J., primary, Hernández‐Martín, A., additional, O'Toole, E.A., additional, Bygum, A., additional, Amaro, C., additional, Aldwin, M., additional, Audouze, A., additional, Bodemer, C., additional, Bourrat, E., additional, Diociaiuti, A., additional, Dolenc‐Voljč, M., additional, Dreyfus, I., additional, El Hachem, M., additional, Fischer, J., additional, Ganemo, A., additional, Gouveia, C., additional, Gruber, R., additional, Hadj‐Rabia, S., additional, Hohl, D., additional, Jonca, N., additional, Ezzedine, K., additional, Maier, D., additional, Malhotra, R., additional, Rodriguez, M., additional, Ott, H., additional, Paige, D.G., additional, Pietrzak, A., additional, Poot, F., additional, Schmuth, M., additional, Sitek, J.C., additional, Steijlen, P., additional, Wehr, G., additional, Moreen, M., additional, Vahlquist, A., additional, Traupe, H., additional, and Oji, V., additional

Published
2019
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2. 先天性鱼鳞病 : 欧洲护理指南, 第二部分

Author

Mazereeuw‐Hautier, J., primary, Hernandez‐Martin, A., additional, O'Toole, E.A., additional, Bygum, A., additional, Amaro, C., additional, Aldwin, M., additional, Audouze, A., additional, Bodemer, C., additional, Bourrat, E., additional, Diociaiuti, A., additional, Dolenc‐Voljc, M., additional, Dreyfus, I., additional, El Hachem, M., additional, Fischer, J., additional, Ganemo, A., additional, Gouveia, C., additional, Gruber, R., additional, Hadj‐Rabia, S., additional, Hohl, D., additional, Jonca, N., additional, Ezzedine, K., additional, Maier, D., additional, Malhotra, R., additional, Rodriguez, M., additional, Ott, H., additional, Paige, D.G., additional, Pietrzak, A., additional, Poot, F., additional, Schmuth, M., additional, Sitek, J.C., additional, Steijlen, P., additional, Wehr, G., additional, Moreen, M., additional, Vahlquist, A., additional, Traupe, H., additional, and Oji, V., additional

Published
2019
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3. Management of congenital ichthyoses: European guidelines of care, part two

Author

Mazereeuw‐Hautier, J., primary, Hernández‐Martín, A., additional, O'Toole, E.A., additional, Bygum, A., additional, Amaro, C., additional, Aldwin, M., additional, Audouze, A., additional, Bodemer, C., additional, Bourrat, E., additional, Diociaiuti, A., additional, Dolenc‐Voljč, M., additional, Dreyfus, I., additional, El Hachem, M., additional, Fischer, J., additional, Ganemo, A., additional, Gouveia, C., additional, Gruber, R., additional, Hadj‐Rabia, S., additional, Hohl, D., additional, Jonca, N., additional, Ezzedine, K., additional, Maier, D., additional, Malhotra, R., additional, Rodriguez, M., additional, Ott, H., additional, Paige, D.G., additional, Pietrzak, A., additional, Poot, F., additional, Schmuth, M., additional, Sitek, J.C., additional, Steijlen, P., additional, Wehr, G., additional, Moreen, M., additional, Vahlquist, A., additional, Traupe, H., additional, and Oji, V., additional

Published
2018
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4. Management of congenital ichthyoses: European guidelines of care, part one

Author

Mazereeuw‐Hautier, J., primary, Vahlquist, A., additional, Traupe, H., additional, Bygum, A., additional, Amaro, C., additional, Aldwin, M., additional, Audouze, A., additional, Bodemer, C., additional, Bourrat, E., additional, Diociaiuti, A., additional, Dolenc‐Voljc, M., additional, Dreyfus, I., additional, El Hachem, M., additional, Fischer, J., additional, Gånemo, A., additional, Gouveia, C., additional, Gruber, R., additional, Hadj‐Rabia, S., additional, Hohl, D., additional, Jonca, N., additional, Ezzedine, K., additional, Maier, D., additional, Malhotra, R., additional, Rodriguez, M., additional, Ott, H., additional, Paige, D.G., additional, Pietrzak, A., additional, Poot, F., additional, Schmuth, M., additional, Sitek, J.C., additional, Steijlen, P., additional, Wehr, G., additional, Moreen, M., additional, O'Toole, E.A., additional, Oji, V., additional, and Hernandez‐Martin, A., additional

Published
2018
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5. Incidence of bullous pemphigoid and pemphigus in Switzerland: a 2-year prospective study

Author

Marazza G, Pham H C, Schärer L, Pedrazzetti P P, Hunziker T, Trüeb R M, Hohl D, Itin P, Lautenschlager S, Naldi L, Borradori L, and Autoimmune bullous disease Swiss study group

Subjects
Adult, Male, Pediatrics, medicine.medical_specialty, Pemphigoid, Adolescent, Population, Dermatology, Young Adult, 030207 dermatology & venereal diseases, 03 medical and health sciences, Age Distribution, 0302 clinical medicine, Pemphigoid, Bullous, medicine, Humans, Prospective Studies, Child, education, Prospective cohort study, Pemphigus foliaceus, Aged, Aged, 80 and over, education.field_of_study, business.industry, Incidence, Incidence (epidemiology), Pemphigus vulgaris, Infant, Newborn, Infant, Middle Aged, medicine.disease, 3. Good health, Surgery, Pemphigus, Child, Preschool, 030220 oncology & carcinogenesis, Female, Bullous pemphigoid, business, Switzerland
Abstract

BACKGROUND: Bullous pemphigoid (BP), pemphigus vulgaris (PV) and pemphigus foliaceus (PF) are autoimmune bullous diseases characterized by the presence of tissue-bound and circulating autoantibodies directed against disease-specific target antigens of the skin. Although rare, these diseases run a chronic course and are associated with significant morbidity and mortality. There are few prospective data on gender- and age-specific incidence of these disorders. OBJECTIVES: Our aims were: (i) to evaluate the incidence of BP and PV/PF in Swiss patients, as the primary endpoint; and (ii) to assess the profile of the patients, particularly for comorbidities and medications, as the secondary endpoint. METHODS: The protocol of the study was distributed to all dermatology clinics, immunopathology laboratories and practising dermatologists in Switzerland. All newly diagnosed cases of BP and pemphigus occurring between 1 January 2001 and 31 December 2002 were collected. In total, 168 patients (73 men and 95 women) with these autoimmune bullous diseases, with a diagnosis based on clinical, histological and immunopathological criteria, were finally included. RESULTS: BP showed a mean incidence of 12.1 new cases per million people per year. Its incidence increased significantly after the age of 70 years, with a maximal value after the age of 90 years. The female/male ratio was 1.3. The age-standardized incidence of BP using the European population as reference was, however, lower, with 6.8 new cases per million people per year, reflecting the ageing of the Swiss population. In contrast, both PV and PF were less frequent. Their combined mean incidence was 0.6 new cases per million people per year. CONCLUSIONS; This is the first comprehensive prospective study analysing the incidence of autoimmune bullous diseases in an entire country. Our patient cohort is large enough to establish BP as the most frequent autoimmune bullous disease. Its incidence rate appears higher compared with other previous studies, most likely because of the demographic characteristics of the Swiss population. Nevertheless, based on its potentially misleading presentations, it is possible that the real incidence rate of BP is still underestimated. Based on its significant incidence in the elderly population, BP should deserve more public health concern.

Published
2009
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7. Increased epidermal expression and absence of mutations inCARD14in a series of patients with sporadic pityriasis rubra pilaris

Author

Eytan, O., primary, Qiaoli, L., additional, Nousbeck, J., additional, van Steensel, M.A.M., additional, Burger, B., additional, Hohl, D., additional, Taïeb, A., additional, Prey, S., additional, Bachmann, D., additional, Avitan-Hersh, E., additional, Jin Chung, H., additional, Shemer, A., additional, Trau, H., additional, Bergman, R., additional, Fuchs-Telem, D., additional, Warshauer, E., additional, Israeli, S., additional, Itin, P.H., additional, Sarig, O., additional, Uitto, J., additional, and Sprecher, E., additional

Published
2014
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12. Novel and recurring ABCA12 mutations associated with harlequin ichthyosis: implications for prenatal diagnosis

Author

Thomas, A.C., primary, Sinclair, C., additional, Mahmud, N., additional, Cullup, T., additional, Mellerio, J.E., additional, Harper, J., additional, Dale, B.A., additional, Turc-Carel, C., additional, Hohl, D., additional, McGrath, J.A., additional, Vahlquist, A., additional, Hellstrom-Pigg, M., additional, Ganemo, A., additional, Metcalfe, K., additional, Mein, C.A., additional, O’Toole, E.A, additional, and Kelsell, D.P., additional

Published
2007
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21. ATP2A2 Mutations in Darier's Disease: Variant Cutaneous Phenotypes Are Associated with Missense Mutations, But Neuropsychiatry Features Are Independent of Mutation Class

Author

Ruiz-Perez, V. L., primary, Carter, S. A., additional, Healy, E., additional, Todd, C., additional, Rees, J. L., additional, Steijlen, P. M., additional, Carmichael, A. J., additional, Lewis, H. M., additional, Hohl, D., additional, Itin, P., additional, Vahlquist, A., additional, Gobello, T., additional, Mazzanti, C., additional, Reggazini, R., additional, Nagy, G., additional, Munro, C. S., additional, and Strachan, T., additional

Published
1999
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