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P Lohse

Showing results (81-90 of 90) with videos related to

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European Journal of Medical Research|December 1, 2001
Sixteen rare sequence variants of the hMLH1 and hMSH2 genes found in a cohort of 254 suspected HNPCC (hereditary non-polyposis colorectal cancer) patients: mutations or polymorphisms?Y Müller-Koch, R Kopp, P Lohse, et al.
Metabolism: Clinical and Experimental|November 1, 1993
Increased production of apolipoprotein A-I associated with elevated plasma levels of high-density lipoproteins, apolipoprotein A-I, and lipoprotein A-I in a patient with familial hyperalphalipoproteinemiaD J Rader, J R Schaefer, P Lohse, et al.
Alimentary Pharmacology & Therapeutics|September 21, 2006
The +1059G/C polymorphism in the C-reactive protein (CRP) gene is associated with involvement of the terminal ileum and decreased serum CRP levels in patients with Crohn's diseaseD Thalmaier, J Dambacher, J Seiderer, et al.
BMJ Case Reports|June 19, 2012
Respiratory distress syndrome due to a novel homozygous ABCA3 mutation in a term neonateHussain Parappil, Ahmad Al Baridi, Sajjad ur Rahman, et al.
Rheumatology (Oxford, England)|March 17, 2004
Periodic fever due to a novel TNFRSF1A mutation in a heterozygous Chinese carrier of MEFV E148QS Stojanov, P Lohse, M F McDermott, et al.
Gut|June 16, 2005
Hereditary non-polyposis colorectal cancer: clinical and molecular evidence for a new entity of hereditary colorectal cancerY Mueller-Koch, H Vogelsang, R Kopp, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|July 11, 2017
Clinical and Molecular Phenotypes of Low-Penetrance Variants of NLRP3: Diagnostic and Therapeutic ChallengesJ B Kuemmerle-Deschner, D Verma, T Endres, et al.
Clinical Genetics|December 17, 2009
Respiratory disease in Niemann-Pick type C2 is caused by pulmonary alveolar proteinosisM Griese, F Brasch, V R Aldana, et al.
Gut|June 16, 2005
Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn's diseaseH-P Török, J Glas, L Tonenchi, et al.
Klinische Padiatrie|October 26, 2013
Genotype-phenotype and genotype-origin correlations in children with mediterranean fever in Germany - an AID-net studyM Jeske, P Lohse, T Kallinich, et al.
Pageof 9

Showing results (81-90 of 90) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 90 results.
European Journal of Medical Research|December 1, 2001
Sixteen rare sequence variants of the hMLH1 and hMSH2 genes found in a cohort of 254 suspected HNPCC (hereditary non-polyposis colorectal cancer) patients: mutations or polymorphisms?Y Müller-Koch, R Kopp, P Lohse, et al.
Metabolism: Clinical and Experimental|November 1, 1993
Increased production of apolipoprotein A-I associated with elevated plasma levels of high-density lipoproteins, apolipoprotein A-I, and lipoprotein A-I in a patient with familial hyperalphalipoproteinemiaD J Rader, J R Schaefer, P Lohse, et al.
Alimentary Pharmacology & Therapeutics|September 21, 2006
The +1059G/C polymorphism in the C-reactive protein (CRP) gene is associated with involvement of the terminal ileum and decreased serum CRP levels in patients with Crohn's diseaseD Thalmaier, J Dambacher, J Seiderer, et al.
BMJ Case Reports|June 19, 2012
Respiratory distress syndrome due to a novel homozygous ABCA3 mutation in a term neonateHussain Parappil, Ahmad Al Baridi, Sajjad ur Rahman, et al.
Rheumatology (Oxford, England)|March 17, 2004
Periodic fever due to a novel TNFRSF1A mutation in a heterozygous Chinese carrier of MEFV E148QS Stojanov, P Lohse, M F McDermott, et al.
Gut|June 16, 2005
Hereditary non-polyposis colorectal cancer: clinical and molecular evidence for a new entity of hereditary colorectal cancerY Mueller-Koch, H Vogelsang, R Kopp, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|July 11, 2017
Clinical and Molecular Phenotypes of Low-Penetrance Variants of NLRP3: Diagnostic and Therapeutic ChallengesJ B Kuemmerle-Deschner, D Verma, T Endres, et al.
Clinical Genetics|December 17, 2009
Respiratory disease in Niemann-Pick type C2 is caused by pulmonary alveolar proteinosisM Griese, F Brasch, V R Aldana, et al.
Gut|June 16, 2005
Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn's diseaseH-P Török, J Glas, L Tonenchi, et al.
Klinische Padiatrie|October 26, 2013
Genotype-phenotype and genotype-origin correlations in children with mediterranean fever in Germany - an AID-net studyM Jeske, P Lohse, T Kallinich, et al.
Pageof 9