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Journal of Lipid Research
|
March 1, 1996
Homozygosity for two point mutations in the lipoprotein lipase (LPL) gene in a patient with familial LPL deficiency: LPL(Asp9-->Asn, Tyr262-->His)
M Rouis, P Lohse, K A Dugi, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
August 13, 2014
Characterization of a partial exon 9/intron 9 deletion in the coagulation factor XII gene (F12) detected in two Turkish families with hereditary angioedema and normal C1 inhibitor
K Bork, K Wulff, J Hardt, et al.
Zeitschrift Fur Gastroenterologie
|
September 9, 2014
[Family with marked hyperferritinemia as a result of hemochromatosis type 4 (ferroportin disease)]
K Muehlenberg, N Faltermeier, P Lohse, et al.
Der Internist
|
July 3, 2010
[38 year-old patient with suspected congenital hormonal dysfunction]
T Bergmann, E G Hahn, P Lohse, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association
|
May 31, 2013
Successful treatment of neonatal respiratory failure caused by a novel surfactant protein C p.Cys121Gly mutation with hydroxychloroquine
N Hepping, M Griese, P Lohse, et al.
Zeitschrift Fur Gastroenterologie
|
October 15, 2013
Cholesteryl ester storage disease: an easily missed diagnosis in oligosymptomatic children
F Freudenberg, P Bufler, R Ensenauer, et al.
The Journal of Biological Chemistry
|
August 4, 1991
Three genetic variants of human plasma apolipoprotein A-IV. apoA-IV-1(Thr347----Ser), apoA-IV-0(Lys167----Glu,Gln360----His), and apoA-IV-3(Glu165----Lys)
P Lohse, M R Kindt, D J Rader, et al.
The Journal of Biological Chemistry
|
August 4, 1990
Human plasma apolipoproteins A-IV-0 and A-IV-3. Molecular basis for two rare variants of apolipoprotein A-IV-1
P Lohse, M R Kindt, D J Rader, et al.
The Journal of Biological Chemistry
|
June 15, 1991
Apolipoprotein E-4Philadelphia (Glu13----Lys,Arg145----Cys). Homozygosity for two rare point mutations in the apolipoprotein E gene combined with severe type III hyperlipoproteinemia
P Lohse, W A Mann, E A Stein, et al.
Clinical Chemistry
|
July 1, 1983
Immunonephelometry of apolipoprotein A-II in hyperlipoproteinemic serum
C C Heuck, I Erbe, K Frech, et al.
Page
of 9
Search research articles
Search
Showing results (21-30 of 90) with videos related to
Sort By:
Page
of 9
Journal of Lipid Research
|
March 1, 1996
Homozygosity for two point mutations in the lipoprotein lipase (LPL) gene in a patient with familial LPL deficiency: LPL(Asp9-->Asn, Tyr262-->His)
M Rouis, P Lohse, K A Dugi, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
August 13, 2014
Characterization of a partial exon 9/intron 9 deletion in the coagulation factor XII gene (F12) detected in two Turkish families with hereditary angioedema and normal C1 inhibitor
K Bork, K Wulff, J Hardt, et al.
Zeitschrift Fur Gastroenterologie
|
September 9, 2014
[Family with marked hyperferritinemia as a result of hemochromatosis type 4 (ferroportin disease)]
K Muehlenberg, N Faltermeier, P Lohse, et al.
Der Internist
|
July 3, 2010
[38 year-old patient with suspected congenital hormonal dysfunction]
T Bergmann, E G Hahn, P Lohse, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association
|
May 31, 2013
Successful treatment of neonatal respiratory failure caused by a novel surfactant protein C p.Cys121Gly mutation with hydroxychloroquine
N Hepping, M Griese, P Lohse, et al.
Zeitschrift Fur Gastroenterologie
|
October 15, 2013
Cholesteryl ester storage disease: an easily missed diagnosis in oligosymptomatic children
F Freudenberg, P Bufler, R Ensenauer, et al.
The Journal of Biological Chemistry
|
August 4, 1991
Three genetic variants of human plasma apolipoprotein A-IV. apoA-IV-1(Thr347----Ser), apoA-IV-0(Lys167----Glu,Gln360----His), and apoA-IV-3(Glu165----Lys)
P Lohse, M R Kindt, D J Rader, et al.
The Journal of Biological Chemistry
|
August 4, 1990
Human plasma apolipoproteins A-IV-0 and A-IV-3. Molecular basis for two rare variants of apolipoprotein A-IV-1
P Lohse, M R Kindt, D J Rader, et al.
The Journal of Biological Chemistry
|
June 15, 1991
Apolipoprotein E-4Philadelphia (Glu13----Lys,Arg145----Cys). Homozygosity for two rare point mutations in the apolipoprotein E gene combined with severe type III hyperlipoproteinemia
P Lohse, W A Mann, E A Stein, et al.
Clinical Chemistry
|
July 1, 1983
Immunonephelometry of apolipoprotein A-II in hyperlipoproteinemic serum
C C Heuck, I Erbe, K Frech, et al.
Page
of 9