L E Carlsson - JoVE Visualize

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Scanning Electron Microscopy|January 1, 1984

Elemental analysis on freeze-dried sections of human skin: studies by electron microprobe and particle induced X-ray emission analysisB Forslind, G M Roomans, L E Carlsson, et al.

Scandinavian Journal of Work, Environment & Health|December 1, 1982

Lead levels determined in Swedish permanent teeth by particle-induced X-ray emissionB Möller, L E Carlsson, G I Johansson, et al.

Tobacco Induced Diseases|July 3, 2009

Impact of genetic polymorphisms on the smoking-related risk of periodontal disease: the population-based study SHIPP Meisel, G Heins, L E Carlsson, et al.

Oral Surgery, Oral Medicine, and Oral Pathology|June 1, 1989

Histologic features of the temporomandibular joint disk and posterior disk attachment: comparison of symptom-free persons with normally positioned disks and patients with internal derangementK Kurita, P L Westesson, N H Sternby, et al.

Thrombosis Research|December 8, 2000

Very low platelet counts in post-transfusion purpura falsely diagnosed as heparin-induced thrombocytopenia. Report of four cases and review of literatureN Lubenow, P Eichler, D Albrecht, et al.

The Plant Cell|April 1, 1995

The tobacco homolog of mammalian calreticulin is present in protein complexes in vivoJ Denecke, L E Carlsson, S Vidal, et al.

Blood|August 26, 1998

Heparin-induced thrombocytopenia: new insights into the impact of the FcgammaRIIa-R-H131 polymorphismL E Carlsson, S Santoso, G Baurichter, et al.

Blood|November 9, 2000

Autosomal-dominant giant platelet syndromes: a hint of the same genetic defect as in Fechtner syndrome owing to a similar genetic linkage to chromosome 22q11-13A Toren, G Rozenfeld-Granot, B Rocca, et al.

American Journal of Human Genetics|October 9, 2001

Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromesK E Heath, A Campos-Barros, A Toren, et al.

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Showing results (11-20 of 19) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 19 results.

Scanning Electron Microscopy|January 1, 1984

Elemental analysis on freeze-dried sections of human skin: studies by electron microprobe and particle induced X-ray emission analysisB Forslind, G M Roomans, L E Carlsson, et al.

Scandinavian Journal of Work, Environment & Health|December 1, 1982

Lead levels determined in Swedish permanent teeth by particle-induced X-ray emissionB Möller, L E Carlsson, G I Johansson, et al.

Tobacco Induced Diseases|July 3, 2009

Impact of genetic polymorphisms on the smoking-related risk of periodontal disease: the population-based study SHIPP Meisel, G Heins, L E Carlsson, et al.

Oral Surgery, Oral Medicine, and Oral Pathology|June 1, 1989

Histologic features of the temporomandibular joint disk and posterior disk attachment: comparison of symptom-free persons with normally positioned disks and patients with internal derangementK Kurita, P L Westesson, N H Sternby, et al.

Thrombosis Research|December 8, 2000

Very low platelet counts in post-transfusion purpura falsely diagnosed as heparin-induced thrombocytopenia. Report of four cases and review of literatureN Lubenow, P Eichler, D Albrecht, et al.

The Plant Cell|April 1, 1995

The tobacco homolog of mammalian calreticulin is present in protein complexes in vivoJ Denecke, L E Carlsson, S Vidal, et al.

Blood|August 26, 1998

Heparin-induced thrombocytopenia: new insights into the impact of the FcgammaRIIa-R-H131 polymorphismL E Carlsson, S Santoso, G Baurichter, et al.

Blood|November 9, 2000

Autosomal-dominant giant platelet syndromes: a hint of the same genetic defect as in Fechtner syndrome owing to a similar genetic linkage to chromosome 22q11-13A Toren, G Rozenfeld-Granot, B Rocca, et al.

American Journal of Human Genetics|October 9, 2001

Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromesK E Heath, A Campos-Barros, A Toren, et al.

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