Publications by Per Teisberg
116 publications found
Original articles
Linkage and association studies with C8A and C8B RFLPs on chromosome 1
Ann Hum Genet, 56 (3), 233-42
DOI 10.1111/j.1469-1809.1992.tb01148.x, PubMed 1360193
Haptoglobin subtypes in Norway and a review of HP subtypes in various populations
Hum Hered, 42 (2), 93-106
DOI 10.1159/000154048, PubMed 1572675
Use of DNA amplification (PCR) and direct DNA sequencing in the characterization of C4 alleles
Ann Hum Genet, 54 (3), 183-9
DOI 10.1111/j.1469-1809.1990.tb00376.x, PubMed 2221823
Genetic aspects of complement component C8 in Norwegian meningococcal disease patients
Scand J Infect Dis, 22 (6), 673-9
DOI 10.3109/00365549009027120, PubMed 2284574
[Use of modern gene technology in forensic medicine]
Tidsskr Nor Laegeforen, 109 (32), 3337-40
PubMed 2574505
Genetic analysis of C4 polymorphism by use of DNA amplification (PCR), allele-specific oligonucleotide probes and allele-specific restriction enzymes
Ann Hum Genet, 53 (3), 221-7
DOI 10.1111/j.1469-1809.1989.tb01788.x, PubMed 2556959
C8A and C8B polymorphisms in Norwegians and Norwegian lapps
Hum Hered, 39 (2), 81-8
DOI 10.1159/000153839, PubMed 2759635
Forensic aspects of haptoglobin: electrophoretic patterns of haptoglobin allotype products and an evaluation of typing procedure
Electrophoresis, 9 (8), 384-92
DOI 10.1002/elps.1150090807, PubMed 2466664
Restriction fragment length polymorphisms of the complement component C4 loci on chromosome 6: studies with emphasis on the determination of gene number
Ann Hum Genet, 52 (2), 77-84
DOI 10.1111/j.1469-1809.1988.tb01082.x, PubMed 2907852
A comparative study on the effect of atenolol and labetalol on exercise capacity and lipid serum levels in essential hypertension
Nephron, 47 Suppl 1, 135-7
DOI 10.1159/000184572, PubMed 3320787
Identification in blood stains through DNA typing with C4 and HLA-DR probes
Z Rechtsmed, 99 (1), 55-64
DOI 10.1007/BF00200369, PubMed 2891229
The C8A and C8B loci are closely linked on chromosome 1
Ann Hum Genet, 50 (2), 139-44
DOI 10.1111/j.1469-1809.1986.tb01032.x, PubMed 3435043
Identification of homozygosity for a human apolipoprotein A-I variant
J Lipid Res, 27 (4), 436-41
PubMed 3723016
EFFECT OF EXERCISE TRAINING IN PATIENTS WITH ESSENTIAL-HYPERTENSION
Acta Med. Scand. (714), 99-103
Effect of exercise training in patients with essential hypertension
Acta Med Scand Suppl, 714, 99-103
DOI 10.1111/j.0954-6820.1986.tb08976.x, PubMed 3472452
HLA genotypes in a family with a case of homozygous C2 deficiency and discoid lupus erythematosus
Acta Derm Venereol, 66 (5), 419-22
PubMed 2431580
Studies of HLA, factor B (Bf), complement C2 and C4 haplotypes in type 1 diabetic and control families from northern Sweden
Hum Hered, 36 (4), 201-12
DOI 10.1159/000153627, PubMed 3639057
Effect of exercise training in patients with essential hypertension
J Hypertens Suppl, 3 (3), S479-81
PubMed 2856772
Genetic polymorphism of complement component C8
Hum Genet, 70 (3), 211-6
DOI 10.1007/BF00273444, PubMed 3879968
HLA-B27 and allotypes of complement components in ankylosing spondylitis
J Rheumatol, 11 (3), 324-6
PubMed 6610755
The two apolipoprotein loci apo A-I and apo A-IV are closely linked in man
Hum Genet, 68 (2), 181-4
DOI 10.1007/BF00279311, PubMed 6500569
The locus for apolipoprotein E (apoE) is close to the Lutheran (Lu) blood group locus on chromosome 19
Hum Genet, 67 (2), 178-82
DOI 10.1007/BF00272996, PubMed 6745937
The in vivo metabolism of C3 in human glomerulonephritis and after renal transplantation
Scand J Clin Lab Invest, 43 (7), 609-16
DOI 10.1080/00365518309168839, PubMed 6361976
Gene order and gene distances in the HLA region studied by the haplotype method
Ann Hum Genet, 47 (4), 285-92
DOI 10.1111/j.1469-1809.1983.tb00998.x, PubMed 6418058
Statement on the nomenclature of human C4 allotypes
Immunobiology, 164 (2), 184-91
DOI 10.1016/s0171-2985(83)80009-6, PubMed 6852863
Genetic studies of an apoA-I lipoprotein variant
Hum Genet, 64 (4), 380-3
DOI 10.1007/BF00292371, PubMed 6413385
The in vivo metabolism of C3 in hepatobiliary disease associated with ulcerative colitis
Scand J Gastroenterol, 17 (4), 523-7
DOI 10.3109/00365528209182243, PubMed 7134879
The in-vivo metabolism of C3 in ankylosing spondylitis
Ann Rheum Dis, 41 (1), 86-9
DOI 10.1136/ard.41.1.86, PubMed 7065734
The locus for apolipoprotein E (apoE) is linked to the complement component C3 (C3) locus on chromosome 19 in man
Hum Genet, 62 (3), 233-6
DOI 10.1007/BF00333526, PubMed 7169215
Fibrinogen gamma chain locus is on chromosome 4 in man
Hum Genet, 61 (1), 24-6
DOI 10.1007/BF00291325, PubMed 6957371
C4 haplotype products and partial inhibition of anti-Rodgers sera
J Immunogenet, 8 (6), 485-91
DOI 10.1111/j.1744-313x.1981.tb00957.x, PubMed 7334218
Complement loci of the HLA complex. Studies on families with intra-HLA crossovers and haplotype associations
Hum Immunol, 2 (3), 247-54
DOI 10.1016/0198-8859(81)90016-1, PubMed 6455398
Genetic heterogeneity in familial lecithin:cholesterol acyltransferase (LCAT) deficiency
Acta Med Scand, 210 (1-2), 1-2
DOI 10.1111/j.0954-6820.1981.tb09766.x, PubMed 7027744
Familial lecithin-cholesterol acyltransferase deficiency in four Norwegian Families. Evidence for low levels of a functionally defective enzyme
Acta Med Scand, 210 (6), 455-9
DOI 10.1111/j.0954-6820.1981.tb09849.x, PubMed 7331892
Familial lecithin:cholesterol acyltransferase deficiency. Report of a fourth family from northwestern Norway
Acta Med Scand, 210 (1-2), 3-6
PubMed 7293825
Association between the electrophoretically-determined C4M haplotype product and partial inhibition of anti-Cha
J Immunogenet, 7 (4), 301-6
DOI 10.1111/j.1744-313x.1980.tb00723.x, PubMed 6161195
The metabolism of C3 in adult coeliac disease
Scand J Gastroenterol, 15 (1), 33-8
DOI 10.3109/00365528009181428, PubMed 7367819
Polymorphism of the sixth component of complement (C6) in Norwegian Lapps
Hum Hered, 30 (4), 211-4
DOI 10.1159/000153130, PubMed 7390511
Further investigations on the genetics of the C+ protein polymorphism
Immunobiology, 158 (1-2), 45-9
DOI 10.1016/s0171-2985(80)80037-4, PubMed 7203519
INTESTINAL MANIFESTATIONS IN BECHTEREWS SYNDROME
Scand. J. Rheumatol. (32), 214-215
A haemolytically non-active C4 gene product
Immunobiology, 158 (1-2), 91-5
DOI 10.1016/s0171-2985(80)80046-5, PubMed 7009412
The C4 system: quantitative studies of different genotypes
Immunobiology, 158 (1-2), 82-5
DOI 10.1016/S0171-2985(80)80044-1, PubMed 6782011
Genetic basis of acquired C4 deficiency
Clin Genet, 16 (5), 297-300
DOI 10.1111/j.1399-0004.1979.tb01005.x, PubMed 519900
Human complement C4 locus is duplicated on some chromosomes
Nature, 279 (5715), 736-7
DOI 10.1038/279736a0, PubMed 450123
Genetic linkage relations of the sixth component of complement (C6)
Hum Genet, 46 (2), 181-92
DOI 10.1007/BF00291920, PubMed 422202
The C4 system: formal and population genetics
Hum Genet, 50 (2), 187-92
DOI 10.1007/BF00390240, PubMed 511133
Metabolic studies of C3 in man
J Immunol Methods, 30 (1), 69-75
DOI 10.1016/0022-1759(79)90274-6, PubMed 512363
Genetic polymorphism of the second component of human complement (C2): presentation of a modified typing technique and data on C2 phenotype distribution, linkage genetics, and haplotype associations a Norwegian family material
Hum Genet, 42 (3), 301-5
DOI 10.1007/BF00291310, PubMed 669711
Hypercatabolism of the third component of complement (C3) in angioimmunoblastic lymphadenopathy
Scand J Haematol, 20 (5), 394-8
DOI 10.1111/j.1600-0609.1978.tb02473.x, PubMed 663553
[Serious complications of cholangiography (Biligram) in lymphoproliferative disorders]
Tidsskr Nor Laegeforen, 98 (6), 305-6
PubMed 635859
Structural complement factor loci and the HLA region
Cytogenet Cell Genet, 22 (1-6), 421-7
DOI 10.1159/000130988, PubMed 752517
The genetic polymorphism of the fourth component of human complement: methodological aspects and a presentation of linkage and association data relevant to its localization in the HLA region
J Exp Med, 146 (5), 1380-9
DOI 10.1084/jem.146.5.1380, PubMed 925607
Very close linkage between HLA-B and Bf inferred from allelic association
Nature, 268 (5620), 527-8
DOI 10.1038/268527a0, PubMed 889587
Nonlinkage between C6 and chromosome 6 markers
Hum Genet, 37 (2), 125-9
DOI 10.1007/BF00393574, PubMed 885533
Properdin factor B (Bf) polymorphism in Norway
Vox Sang, 32 (1), 52-5
DOI 10.1111/j.1423-0410.1977.tb00603.x, PubMed 841963
Complement system studies in adult coeliac disease
Scand J Gastroenterol, 12 (7), 873-6
DOI 10.3109/00365527709181733, PubMed 594655
Genetic polymorphism of C4 in man and localisation of a structural C4 locus to the HLA gene complex of chromosome 6
Nature, 264 (5583), 253-4
DOI 10.1038/264253a0, PubMed 1088823
ESD polymorphism in Norway
Hum Genet, 34 (1), 63-4
DOI 10.1007/BF00284436, PubMed 965006
[Letter: Use of naloxone (Narcan) in poisoning by morphine, methadone and dextro propoxyphene]
Tidsskr Nor Laegeforen, 96 (17-18), 1007-8
PubMed 985995
[Bleeding esophageal varices. Diagnosis and treatment]
Tidsskr Nor Laegeforen, 96 (8), 512-5
PubMed 1083080
GLO polymorphism in Norway
Hum Hered, 26 (6), 454-7
DOI 10.1159/000152840, PubMed 1010527
Bf locus and the HLA region
Birth Defects Orig Artic Ser, 12 (7), 345-6
PubMed 1024638
Bf locus and the HLA region
Cytogenet Cell Genet, 16 (1-5), 345-6
DOI 10.1159/000130628, PubMed 975905
The Bf locus in the HLA region of chromosome 6: linkage and association studies
Humangenetik, 30 (4), 291-6
DOI 10.1007/BF00275141, PubMed 1218859
In vivo activation of C3 revealed by crossed immunoelectrophoresis as a parameter of immunological activity in disease
Clin Chim Acta, 62 (1), 35-41
DOI 10.1016/0009-8981(75)90277-6, PubMed 1170962
On the localization of the Gb locus within the MHS region of chromosome No. 6
Tissue Antigens, 5 (4), 257-61
DOI 10.1111/j.1399-0039.1975.tb01472.x, PubMed 1154360
Complement system studies in systemic lupus erythematosus (SLE)
Acta Med Scand, 197 (1-2), 131-4
DOI 10.1111/j.0954-6820.1975.tb04890.x, PubMed 47697
Humoral immune system activity in inflammatory bowel disease
Scand J Gastroenterol, 10 (5), 545-9
PubMed 1171519
Genetics of LCAT (lecithin: cholesterol acyltransferase) deficiency
Ann Hum Genet, 38 (3), 327-31
DOI 10.1111/j.1469-1809.1975.tb00617.x, PubMed 806250
Probable linkage of LCAT locus in man to the alpha haptoglobin locus on chromosome 16
Nature, 249 (457), 550-1
DOI 10.1038/249550a0, PubMed 4834078
FAMILIAL LECITHIN-CHOLESTEROL ACYLTRANSFERASE DEFICIENCY - REPORT OF A THIRD NORWEGIAN FAMILY WITH 2 AFFLICTED MEMBERS
Scand. J. Clin. Lab. Invest., 33 137, 101-105
DOI 10.3109/00365517409100637
IMMUNOLOGICAL HEREDITARY NEPHROPATHY
Acta Med. Scand. (571), 1-28
Familial lecithin:cholesterol acyltransferase deficiency. Report of a third Norwegian family with two afflicted members
Scand J Clin Lab Invest Suppl, 137, 101-5
PubMed 4367609
C3 polymorphism: genetic linkage relations
Clin Genet, 6 (1), 66-72
DOI 10.1111/j.1399-0004.1974.tb00632.x, PubMed 4426132
[Halothane-hepatitis. A case report]
Tidsskr Nor Laegeforen, 93 (35), 2567-9
PubMed 4772805
In-vivo activation of complement in hereditary nephropathy
Lancet, 2 (7825), 356-8
DOI 10.1016/s0140-6736(73)93194-2, PubMed 4124530
Circulating conversion products of C3 in liver disease. Evidence for in vivo activation of the complement system
Clin Exp Immunol, 14 (4), 509-14
PubMed 4201114
Heart pathology in chronic alcoholism
Acta Pathol Microbiol Scand A, 81 (3), 315-22
DOI 10.1111/j.1699-0463.1973.tb03540.x, PubMed 4767225
Red cell acid phosphatase polymorphism in Norway
Hum Hered, 23 (3), 257-62
DOI 10.1159/000152583, PubMed 4760582
Primary pulmonary hypertension in infancy
Acta Paediatr Scand, 62 (1), 69-72
DOI 10.1111/j.1651-2227.1973.tb08068.x, PubMed 4691258
HEART PATHOLOGY IN CHRONIC ALCOHOLISM
ACTA PATH MICRO IM A, A 81 (3), 315-322
Application of the C3 system in paternity cases
Vox Sang, 22 (3), 213-21
DOI 10.1111/j.1423-0410.1972.tb05194.x, PubMed 5019390
Erythrocyte alanine aminotransferase polymorphism in Norwegian Lapps
Hum Hered, 22 (4), 380-6
DOI 10.1159/000152514, PubMed 4647204
Transferrin variants in Norway
Hum Hered, 22 (3), 259-63
DOI 10.1159/000152496, PubMed 5079052
[Fatal poisoning by d-propoxyphene]
Tidsskr Nor Laegeforen, 91 (27), 1938-9
PubMed 5115789
[Lobar pneumonia as a cause of sudden death]
Tidsskr Nor Laegeforen, 91 (21), 1539-40
PubMed 5569813
The conversion rate of human C3 under different storage conditions
Vox Sang, 20 (3), 230-8
DOI 10.1111/j.1423-0410.1971.tb00434.x, PubMed 5093553
Another variant in the C 3 system
Clin Genet, 2 (5), 298-302
DOI 10.1111/j.1399-0004.1971.tb00290.x, PubMed 4112057
Genetics of the C 3 system. Family, mother-child and association studies
Hum Hered, 21 (5), 458-66
DOI 10.1159/000152438, PubMed 4112280
The distribution of C 3 types in Norway
Hum Hered, 21 (2), 154-61
DOI 10.1159/000152395, PubMed 4108382
HL-A polymorphism of Norwegian Lapps
Tissue Antigens, 1 (3), 137-46
DOI 10.1111/j.1399-0039.1971.tb00090.x, PubMed 4116443
Serum protein polymorphisms among Norwegian Lapps. Studies on the Lp, Ag, Gc and transferrin systems
Hum Hered, 21 (2), 134-9
DOI 10.1159/000152393, PubMed 5127405
C 3 types of Norwegian Lapps
Hum Hered, 21 (2), 162-7
DOI 10.1159/000152396, PubMed 4108383
High voltage agarose gel electrophoresis in the study of C 3 polymorphism
Vox Sang, 19 (1), 47-56
DOI 10.1111/j.1423-0410.1970.tb01494.x, PubMed 5488658
New variants in the C3 system
Hum Hered, 20 (6), 631-7
DOI 10.1159/000152369, PubMed 5514302
Immunosuppressive therapy in Wegener's granulomatosis
Acta Med Scand, 187 (1-2), 7-9
DOI 10.1111/j.0954-6820.1970.tb02899.x, PubMed 5423209
[Sudden death in bronchial asthma]
Tidsskr Nor Laegeforen, 89 (19), 1488-91
PubMed 5383700
[Mefrusid (Baycaron)--a new diuretic in Norway]
Tidsskr Nor Laegeforen, 89 (18), 1431
PubMed 5376305
[Hyperuricemia in therapy with saluretics]
Tidsskr Nor Laegeforen, 89 (13), 1110-1
PubMed 5799901
[Spontaneous mediastinal emphysema]
Tidsskr Nor Laegeforen, 88 (19), 1748-9
PubMed 5700513
Review articles
[Which cholesterol-lowering drugs should be used in the primary prevention of cardiovascular disease?]
Tidsskr Nor Laegeforen, 122 (23), 2287-8
PubMed 12448270
[Guidelines for pharmacological primary prevention of cardiovascular diseases--who should be treated?]
Tidsskr Nor Laegeforen, 122 (23), 2277-81
PubMed 12448268
[Which antihypertensive drugs should be used in the primary prevention of cardiovascular disease?]
Tidsskr Nor Laegeforen, 122 (23), 2283-6
PubMed 12448269
The genetic background of anticipation
J R Soc Med, 88 (4), 185-7
PubMed 7745561
[Clinical significance of serum complement investigation]
Tidsskr Nor Laegeforen, 94 (1), 24-9
PubMed 4595244
Other articles
[Shortcomings and strength of practice guidelines]
Tidsskr Nor Laegeforen, 123 (11), 1566-7
PubMed 12822025
Disease caused by expanding genes
J Intern Med, 236 (1), 1-2
DOI 10.1111/j.1365-2796.1994.tb01112.x, PubMed 8021565
Genetics of non-insulin-dependent diabetes mellitus (NIDDM)
J Intern Med, 234 (5), 439-40
DOI 10.1111/j.1365-2796.1993.tb00774.x, PubMed 8228786
A BamHI RFLP of the C8A gene
Nucleic Acids Res, 19 (13), 3762
DOI 10.1093/nar/19.13.3762-a, PubMed 1677187
A BamH1 RFLP of the C8B gene
Nucleic Acids Res, 17 (16), 6760
DOI 10.1093/nar/17.16.6760, PubMed 2571125
A structural locus for coagulation factor XIIIA (F13A) is located distal to the HLA region on chromosome 6p in man
Am J Hum Genet, 37 (1), 215-20
PubMed 2858156
Electrophoretic polymorphism of human C4 is due to charge differences in the alpha chain, presumably in the C4d fragment
Scand J Immunol, 14 (3), 303-7
DOI 10.1111/j.1365-3083.1981.tb00568.x, PubMed 7330601
Serial complement studies in a patient with Goodpasture's syndrome treated with bilateral nephrectomy and renal transplantation
Am J Med, 59 (4), 563-7
DOI 10.1016/0002-9343(75)90263-6, PubMed 1101681
Books
Pasientvolum og behandlingskvalitet: metodevurdering basert på egen og internasjonal litteraturgransking
In SMM-rapport, Senteret, Oslo, nr 2/2001, 137 s.
BIBSYS 010654372, ISBN 82-14-02407-2
Abstracts of papers presented at the 36.Scandinavian congress of internal medicine: June 1-3, 1978, Oslo, Norway
In Acta medica Scandinavica, Supplementum, Almqvist & Wiksell, Stockholm, 621, 48 s.
BIBSYS 011166894
Theses
Studies on the C 3 system of human serum
Oslo, 1 b. (flere pag.)
BIBSYS 940351811