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Psychiatrie, Neurologie, Und Medizinische Psychologie|November 1, 1989
[Etiologic and pathogenetic aspects of the demyelinating process in multiple sclerosis]R M Schmidt, V Neumann, B Kissig, et al.
Clinical Chemistry|May 1, 1976
Use of blood specimens collected on filter paper in screening for abnormal hemoglobinsR M Schmidt, E M Brosious, S Holland, et al.
American Journal of Clinical Pathology|August 1, 1976
Hemoglobin Bethesda, beta 145 (HC2) Tyr replaced by His, in a Canadian familyR M Schmidt, D L Jue, M A Ali, et al.
Circulation|March 29, 2000
A newly created splice donor site in exon 25 of the MyBP-C gene is responsible for inherited hypertrophic cardiomyopathy with incomplete disease penetranceJ A Moolman, S Reith, K Uhl, et al.
The Journal of Biological Chemistry|December 10, 1976
Hemoglobin Providence. A human hemoglobin variant occurring in two forms in vivoW F Moo-Penn, D L Jue, K C Bechtel, et al.
Hemoglobin|January 1, 1977
Hemoglobin Lufkin: beta 29 (B11) Gly replaced by Asp. An unstable hemoglobin variant involving an internal amino acid residueR M Schmidt, K C Bechtel, M H Johnson, et al.
Biomedizinische Technik. Biomedical Engineering|January 1, 1994
[Torsion stability of coronary catheters]R Bach, F Jung, R M Schmidt, et al.
The American Journal of Surgical Pathology|July 1, 1987
A classification of cardiac allograft rejection. A modification of the classification by BillinghamJ Kemnitz, T Cohnert, H J Schäfers, et al.
Biochimica Et Biophysica Acta|February 22, 1977
Hemoglobin Tarrant: alpha126(H9) Asp leads to Asn. A new hemoglobin variant in the alpha1beta1 contact region showing high oxygen affinity and reduced cooperativityW F Moo-Penn, D L Jue, M H Johnson, et al.
Blood|September 1, 1975
The presence of hemoglobin S and C Harlem in an individual in the United StatesW Moo-Penn, K Bechtel, D Jue, et al.
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