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S Heilmann

Showing results (21-30 of 38) with videos related to

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Schweizerische Medizinische Wochenschrift. Supplementum|January 1, 1984
[Prognostic significance of the QT-interval following myocardial infarction]M H Hust, S Heilmann, T Bonzel, et al.
Chiropractic & Manual Therapies|August 20, 2025
Variation in use of radiographs in chiropractic care: a cross-sectional studyR K Jensen, S Heilmann, J N Thomsen, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|November 12, 2003
Clinical presentation of qualitative olfactory dysfunctionJ Frasnelli, B N Landis, S Heilmann, et al.
The British Journal of Dermatology|March 2, 2013
No genetic support for a contribution of prostaglandins to the aetiology of androgenetic alopeciaS Heilmann, D R Nyholt, F F Brockschmidt, et al.
Dermatologische Monatschrift|June 1, 1980
[Photochemotherapy of psoriasis using 8-MOP and UVA. Results of interval treatment. Clinical experiences from 6 dermatology hospitals]D Metz, H Meffert, J Barth, et al.
The British Journal of Dermatology|March 5, 2010
Fine mapping of the human AR/EDA2R locus in androgenetic alopeciaF F Brockschmidt, A M Hillmer, S Eigelshoven, et al.
The British Journal of Dermatology|May 25, 2013
Evidence for a polygenic contribution to androgenetic alopeciaS Heilmann, F F Brockschmidt, A M Hillmer, et al.
The Journal of Prevention of Alzheimer'S Disease|January 31, 2022
Association between 9p21-23 Locus and Frailty in a Community-Dwelling Greek Population: Results from the Hellenic Longitudinal Investigation of Ageing and DietN Mourtzi, A Hatzimanolis, G Xiromerisiou, et al.
Clinical Genetics|September 20, 2017
Common variants in DLG1 locus are associated with non-syndromic cleft lip with or without cleft palateA Mostowska, A Gaczkowska, K Żukowski, et al.
Molecular Syndromology|April 10, 2014
Microdeletions including FMR1 in three female patients with intellectual disability - further delineation of the phenotype and expression studiesA M Zink, E Wohlleber, H Engels, et al.
Pageof 4

Showing results (21-30 of 38) with videos related to

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Pageof 4
Schweizerische Medizinische Wochenschrift. Supplementum|January 1, 1984
[Prognostic significance of the QT-interval following myocardial infarction]M H Hust, S Heilmann, T Bonzel, et al.
Chiropractic & Manual Therapies|August 20, 2025
Variation in use of radiographs in chiropractic care: a cross-sectional studyR K Jensen, S Heilmann, J N Thomsen, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|November 12, 2003
Clinical presentation of qualitative olfactory dysfunctionJ Frasnelli, B N Landis, S Heilmann, et al.
The British Journal of Dermatology|March 2, 2013
No genetic support for a contribution of prostaglandins to the aetiology of androgenetic alopeciaS Heilmann, D R Nyholt, F F Brockschmidt, et al.
Dermatologische Monatschrift|June 1, 1980
[Photochemotherapy of psoriasis using 8-MOP and UVA. Results of interval treatment. Clinical experiences from 6 dermatology hospitals]D Metz, H Meffert, J Barth, et al.
The British Journal of Dermatology|March 5, 2010
Fine mapping of the human AR/EDA2R locus in androgenetic alopeciaF F Brockschmidt, A M Hillmer, S Eigelshoven, et al.
The British Journal of Dermatology|May 25, 2013
Evidence for a polygenic contribution to androgenetic alopeciaS Heilmann, F F Brockschmidt, A M Hillmer, et al.
The Journal of Prevention of Alzheimer'S Disease|January 31, 2022
Association between 9p21-23 Locus and Frailty in a Community-Dwelling Greek Population: Results from the Hellenic Longitudinal Investigation of Ageing and DietN Mourtzi, A Hatzimanolis, G Xiromerisiou, et al.
Clinical Genetics|September 20, 2017
Common variants in DLG1 locus are associated with non-syndromic cleft lip with or without cleft palateA Mostowska, A Gaczkowska, K Żukowski, et al.
Molecular Syndromology|April 10, 2014
Microdeletions including FMR1 in three female patients with intellectual disability - further delineation of the phenotype and expression studiesA M Zink, E Wohlleber, H Engels, et al.
Pageof 4