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Peter Lohse

Showing results (1-10 of 121) with videos related to

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Indian Journal of Human Genetics|November 20, 2012
Crigler-Najjar syndrome type 2: Novel UGT1A1 mutationKarippoth Mohandas Nair, Peter Lohse, Sheela Nampoothiri
Clinical and Experimental Rheumatology|September 26, 2013
Macrophage activation syndrome as the initial manifestation of tumour necrosis factor receptor 1-associated periodic syndrome (TRAPS)Gerd Horneff, Asma Rhouma, Carola Weber, et al.
Human Genetics|March 27, 2003
Autosomal dominant malignant and catecholamine-producing paraganglioma caused by a splice donor site mutation in SDHCStephan Niemann, Ulrich Müller, Dieter Engelhardt, et al.
American Journal of Clinical Pathology|July 18, 2003
Insulin-like growth factor-I receptor and PTEN protein expression in endometrial carcinoma. Correlation with bax and bcl-2 expression, microsatellite instability status, and outcomeGloria Peiró, Peter Lohse, Doris Mayr, et al.
European Journal of Pediatrics|September 15, 2004
Multiple pheochromocytomas and paragangliomas in a young patient carrying a SDHD gene mutationAstrid Novosel, Alfred Heger, Peter Lohse, et al.
Pediatrics|July 3, 2004
A novel CIAS1 mutation and plasma/cerebrospinal fluid cytokine profile in a German patient with neonatal-onset multisystem inflammatory disease responsive to methotrexate therapySilvia Stojanov, Michael Weiss, Peter Lohse, et al.
Journal of the American Academy of Dermatology|July 13, 2011
Pyoderma gangrenosum, acne, and suppurative hidradenitis (PASH)--a new autoinflammatory syndrome distinct from PAPA syndromeMarkus Braun-Falco, Oleksandr Kovnerystyy, Peter Lohse, et al.
American Journal of Reproductive Immunology (New York, N.Y. : 1989)|June 24, 2004
Vasoconstrictively acting AT1R A1166C and NOS3 4/5 polymorphisms in recurrent spontaneous abortions (RSA)Tina Buchholz, Peter Lohse, Elke Kosian, et al.
Expert Opinion on Pharmacotherapy|July 29, 2006
Genetic variants and the risk of Crohn's disease: what does it mean for future disease management?Helga-Paula Török, Jürgen Glas, Peter Lohse, et al.
Digestive Diseases (Basel, Switzerland)|January 31, 2004
Alterations of the CARD15/NOD2 gene and the impact on management and treatment of Crohn's disease patientsHelga-Paula Török, Jürgen Glas, Peter Lohse, et al.
Pageof 13

Showing results (1-10 of 121) with videos related to

Sort By:
Pageof 13
Indian Journal of Human Genetics|November 20, 2012
Crigler-Najjar syndrome type 2: Novel UGT1A1 mutationKarippoth Mohandas Nair, Peter Lohse, Sheela Nampoothiri
Clinical and Experimental Rheumatology|September 26, 2013
Macrophage activation syndrome as the initial manifestation of tumour necrosis factor receptor 1-associated periodic syndrome (TRAPS)Gerd Horneff, Asma Rhouma, Carola Weber, et al.
Human Genetics|March 27, 2003
Autosomal dominant malignant and catecholamine-producing paraganglioma caused by a splice donor site mutation in SDHCStephan Niemann, Ulrich Müller, Dieter Engelhardt, et al.
American Journal of Clinical Pathology|July 18, 2003
Insulin-like growth factor-I receptor and PTEN protein expression in endometrial carcinoma. Correlation with bax and bcl-2 expression, microsatellite instability status, and outcomeGloria Peiró, Peter Lohse, Doris Mayr, et al.
European Journal of Pediatrics|September 15, 2004
Multiple pheochromocytomas and paragangliomas in a young patient carrying a SDHD gene mutationAstrid Novosel, Alfred Heger, Peter Lohse, et al.
Pediatrics|July 3, 2004
A novel CIAS1 mutation and plasma/cerebrospinal fluid cytokine profile in a German patient with neonatal-onset multisystem inflammatory disease responsive to methotrexate therapySilvia Stojanov, Michael Weiss, Peter Lohse, et al.
Journal of the American Academy of Dermatology|July 13, 2011
Pyoderma gangrenosum, acne, and suppurative hidradenitis (PASH)--a new autoinflammatory syndrome distinct from PAPA syndromeMarkus Braun-Falco, Oleksandr Kovnerystyy, Peter Lohse, et al.
American Journal of Reproductive Immunology (New York, N.Y. : 1989)|June 24, 2004
Vasoconstrictively acting AT1R A1166C and NOS3 4/5 polymorphisms in recurrent spontaneous abortions (RSA)Tina Buchholz, Peter Lohse, Elke Kosian, et al.
Expert Opinion on Pharmacotherapy|July 29, 2006
Genetic variants and the risk of Crohn's disease: what does it mean for future disease management?Helga-Paula Török, Jürgen Glas, Peter Lohse, et al.
Digestive Diseases (Basel, Switzerland)|January 31, 2004
Alterations of the CARD15/NOD2 gene and the impact on management and treatment of Crohn's disease patientsHelga-Paula Török, Jürgen Glas, Peter Lohse, et al.
Pageof 13