Published in Radiol Diagn (Berl) on January 01, 1977
[The blood vessels of the posterior cranial fossa. anatomy, pathophysiology, clinic--a survey (author's transl)]. Arch Otorhinolaryngol (1978) 0.79
Polymorphism of red cell glyoxalase I (EI: 4.4.1.5); a new genetic marker in man. Investigation of 169 mother-child combinations. Humangenetik (1975) 3.47
Heterozygous mutations in ANKH, the human ortholog of the mouse progressive ankylosis gene, result in craniometaphyseal dysplasia. Nat Genet (2001) 2.39
Dynamics of mitotic spindle organization and function. Soc Gen Physiol Ser (1975) 2.07
Mitosis in Barbulanympha. II. Dynamics of a two-stage anaphase, nuclear morphogenesis, and cytokinesis. J Cell Biol (1978) 1.37
The use of dietary fiber in the management of simple, childhood, idiopathic, recurrent, abdominal pain. Results in a prospective, double-blind, randomized, controlled trial. Am J Dis Child (1985) 1.29
[On balance of polymorphism of haptoglobins]. Humangenetik (1966) 1.26
Mitosis in Barbulanympha. I. Spindle structure, formation, and kinetochore engagement. J Cell Biol (1978) 1.19
Adenosine deaminase polymorphism (EC: 3.5.4.4): formal genetics and linkage relations. Humangenetik (1969) 1.12
Sexual violence in post-conflict Liberia: survivors and their care. Trop Med Int Health (2012) 1.09
The selenium state of children. II. Selenium content of serum, whole blood, hair and the activity of erythrocyte glutathione peroxidase in dietetically treated patients with phenylketonuria and maple-syrup-urine disease. Eur J Pediatr (1978) 1.04
On the computations analyzing natural optic flow: quantitative model analysis of the blowfly motion vision pathway. J Neurosci (2005) 1.03
Polymorphism of alanine aminotransferase (E.C.2.7.6.1): common and rare alleles. Hum Genet (1979) 1.03
A principle for the formation of the spatial structure of cortical feature maps. Proc Natl Acad Sci U S A (1990) 1.03
Adaptive color segmentation-a comparison of neural and statistical methods. IEEE Trans Neural Netw (1997) 1.02
Comparative clinical trial of granisetron and ondansetron in the prophylaxis of cisplatin-induced emesis. The Granisetron Study Group. J Clin Oncol (1995) 1.01
Nearby stop codons in exons of the neurofibromatosis type 1 gene are disparate splice effectors. Am J Hum Genet (1998) 1.00
Genetic analysis of a sarcoma accidentally transplanted from a patient to a surgeon. N Engl J Med (1996) 0.94
[A homeotherapeutic double-blind experiment and its problems]. Hippokrates (1966) 0.93
PGM1 subtyping by means of acid starch gel electrophoresis. Hum Genet (1978) 0.91
Human mitochondrial glutamic-oxaloacetic-transaminase, GOTM: formal genetics. Hum Genet (1979) 0.91
Population genetics of adenosine deaminase (EC: 3.5.4.4): gene frequencies in Southwestern Germany. Humangenetik (1969) 0.91
Transspecific variability of soluble glutamic-pyruvic transaminase in primates. Humangenetik (1975) 0.89
Sex-linked AFLP markers indicate a pseudoautosomal region in hemp ( Cannabis sativa L.). Theor Appl Genet (2003) 0.87
Polyploidization in the fish family Cyprinidae, order Cypriniformes. I. DNA-content and chromosome sets in various species of Cyprinidae. Humangenetik (1969) 0.85
[Critique of a total knee prosthesis, its construction, functioning and clinical approbation (the Guépar prosthesis) (author's transl)]. Arch Orthop Unfallchir (1974) 0.84
Disambiguating complex visual information: towards communication of personal views of a scene. Perception (1996) 0.84
Red cell glyoxalase i (E.C.: 4.4.1.5): formal genetics and linkage relations. Humangenetik (1975) 0.83
[Circulation of generally not recognized therapeutic procedures in private practice. Results of a 3d conclusive enquiry]. Med Welt (1971) 0.83
A competitive-layer model for feature binding and sensory segmentation. Neural Comput (2001) 0.83
Antenatal records: do they help us? A new record for watching fetal growth. Trop Doct (1984) 0.82
Red-cell uridine-5-monophosphate kinase (UMPK): formal genetics, linkage analysis and population genetics from southwestern Germany. Humangenetik (1975) 0.82
Chromosome 18 replaced by two ring chromosomes of chromosome 18 origin. Hum Genet (2003) 0.82
Genetic polymorphism of mannosephosphate isomerase in Primates. Humangenetik (1973) 0.81
[On the formal genetics of isoenzymes, using 6-PGD (EC:1.1.1.44) as an example]. Humangenetik (1969) 0.81
Identification of highly polymorphic microsatellites in the rhesus macaque Macaca mulatta by cross-species amplification. Mol Ecol (1996) 0.81
Genetics and linkage analysis on adenylate kinase. Humangenetik (1971) 0.81
Linkage between the loci for mitochondrial malic enzyme (ME2) and coagulation factor XIIIA subunit (F13A). Hum Genet (1985) 0.81
Aminoaciduria in progressive muscular dystrophy. A family study. Ger Med Mon (1967) 0.81
Duplication of the LDH gene loci by polyploidization in the fish order Clupeiformes. Humangenetik (1968) 0.81
[Our clinical experiences with Guépar total knee prosthesis (author's transl)]. Arch Orthop Unfallchir (1974) 0.80
ABO blood groups , Inv serum groups, and serum proteins in leprosy patients from West Bengal (India). Humangenetik (1971) 0.80
[The formal genetics of adenylate kinase (EC: 2.7.4.3); evidence for linkage between the loci for AK and ABO]. Humangenetik (1969) 0.80
Substrate affinity in PGM1, PGM2, and PGM2 isozymes. Hum Genet (1980) 0.80
Deletion of short arm of a chromosome 18 (46, XX, 18 p-). Humangenetik (1967) 0.80
Mitochondrial malic enzyme (E.C.1.1.1.40) in human leukocytes: formal genetics and population genetics. Hum Genet (1979) 0.79
The joint development of orientation and ocular dominance: role of constraints. Neural Comput (1997) 0.79
[Gonadal doses in radiation therapy of non-tumorous diseases]. Radiobiol Radiother (Berl) (1965) 0.79
Crassulacean acid metabolism (CAM) in leaves of Aloe arborescens mill : Comparative studies of the carbon metabolism of chlorenchym and central hydrenchym. Planta (1979) 0.79
New mutation in a Swiss girl leading to clinical and biochemical beta-thalassemia minor. Humangenetik (1973) 0.79
[Formal genetics and population genetics of Inv polymorphism]. Blut (1966) 0.79
[On the problem of assigning genes to definite human autosomes with the aid of chromosome aberrations]. Humangenetik (1967) 0.78
Determination of free apolipoprotein(a) in serum by immunoassay and its significance for risk assessment in patients with coronary artery disease. Clin Chem Lab Med (1999) 0.78
[Value of Dimer-X myelography in the diagnosis of lumbar intravertebral disk lesions]. Zentralbl Neurochir (1977) 0.78
[Meningeomas in childhood and adolescence]. Beitr Neurochir (1968) 0.78
Aminolevulinate dehydratase (E.C. 4.2.1.24): linkage analysis. Hum Genet (1982) 0.77
[Radiotherapy of humeroscapular periarthritis]. Radiobiol Radiother (Berl) (1972) 0.77
A fluid system for the cultivation, light microscope examination and manipulation of obligate anaerobes. J Protozool (1974) 0.77
Electrophoretic and isoelectric focusing studies in Brazilian Indians: data on four systems. Hum Biol (1989) 0.77
Genetic polymorphism of inter-alpha-trypsin-inhibitor (ITI): formal genetic and linkage analyses. Hum Genet (1991) 0.77
Lactate dehydrogenase: inhibition of subunit A by the sulfhydryl reagent AgNO3. Humangenetik (1975) 0.77
In vitro studies on the interaction between bile salts and key enzymes of the liver. Klin Wochenschr (1982) 0.77
[On the population genetics of acid phosphatase in erythrocytes (E C 3.1.3.2.): phenotype and allele frequency in Southwestern Germany]. Humangenetik (1968) 0.76
Nerve suture without tension, a method for repairing transected peripheral nerves. Acta Neurochir (Wien) (1976) 0.76
[Examinations about the polymorphism of red blood cell acid phosphatase (E C 3.1.3.2.)]. Humangenetik (1966) 0.76
D3S1358: sequence analysis and gene frequency in a German population. Forensic Sci Int (1998) 0.75
Linkage analysis in granular corneal dystrophy (Groenouw I), Schnyder's crystalline corneal dystrophy, and Reis-Bücklers' corneal dystrophy. Graefes Arch Clin Exp Ophthalmol (1989) 0.75
[Space-demanding intracranial processes in puerperium (author's transl)]. Zentralbl Gynakol (1979) 0.75
Factors influencing the growth and maintenance of tubed cultures of embryonic chick cells. Appl Microbiol (1968) 0.75
DNA-fingerprinting: a further note on mutation rates. Hum Genet (1992) 0.75
Dynamical stability conditions for recurrent neural networks with unsaturating piecewise linear transfer functions. Neural Comput (2001) 0.75
Initial experiences with a total knee prosthesis implanted without bone cement. Arch Orthop Trauma Surg (1979) 0.75
Polymorphism of glucose dehydrogenase (GDH, EC 1.1.1.47): formal and population genetic data. Hum Genet (1993) 0.75
[Prevalence of generally not accepted therapeutic procedures in free practice. Result of a second poll]. Z Allgemeinmed (1969) 0.75
[On the trans-specific evolution of proteins]. Humangenetik (1968) 0.75
[Populationgenetics of phosphoglucoseisomerase. (EC:5.3.1.9)]. Humangenetik (1971) 0.75
On the question of genetic linkage between the structural loci for ABO and Gc. Humangenetik (1968) 0.75
[Surgical technic and problems of retentio testis inguinalis and abdominalis]. Bruns Beitr Klin Chir (1969) 0.75
[Medical art as an obstacle]. Landarzt (1965) 0.75
[Can a homeopathic approach still be meaningful in our practical thinking and action of today?]. Landarzt (1966) 0.75
[The diagnostic predicability of electronic pulse oscillography in peripheral arterial circulation disorders]. Z Arztl Fortbild (Jena) (1970) 0.75
[Age and cause of death of American physicians?]. Med Welt (1970) 0.75
Genetic polymorphism of isocitrate dehydrogenase in Primates. Humangenetik (1973) 0.75
[Transspecific variability of lactate dehydrogenases (E.C.: 1.1.1.27) in mammals]. Humangenetik (1970) 0.75
[Genetics of 6-phosphogluconate dehydrogenase (EC:1.1.1.44): a new variant F (Freiburg)]. Humangenetik (1970) 0.75
[Erythrocyte enzymes of primates. Adenylate kinase; EC:2.7.4.3]. Humangenetik (1971) 0.75
[Lymphocyte transformation in chronic hepatitis and other hepatic diseases]. Arch Klin Med (1969) 0.75
[The case-history in general practice]. Munch Med Wochenschr (1970) 0.75
Polymorphism of the phosphotransferases adenylate kinase and pyruvate kinase. Existence of a common subunit? Humangenetik (1968) 0.75
[Amino acid plotting charts in progressive muscular dystrophy. Family studies]. Dtsch Med Wochenschr (1966) 0.75
[Hemodynamic changes in the post-thrombotic syndrome]. Z Gesamte Inn Med (1973) 0.75
[Studies on population genetics of haptoglobin subgroups]. Blut (1966) 0.75
[Genetically determined variants of NADH-diaphorase]. Humangenetik (1970) 0.75
Hereditary methemoglobinemia associated with NADH diaphorase deficiency. Humangenetik (1973) 0.75
[Extracranial vertebral artery aneurysm]. Zentralbl Chir (1970) 0.75
[Problematic mother-child exclusion with PGM1]. Humangenetik (1971) 0.75
[On the population genetics of adenylate kinase: gene frequency in a Southwestern German sample]. Humangenetik (1968) 0.75
Population genetics of red cell phosphoglucomutase (E C 2.7.5.1): gene frequencies in Southwestern Germany. Humangenetik (1968) 0.75
[Angiomatous malformation in the region of the pelvis minor]. Zentralbl Gynakol (1969) 0.75
[Polyploidization in the fish family cyprinidae. Duplication of the gene loci for NAD-dependent malate dehydrogenase]. Humangenetik (1971) 0.75
[Recurrence and responsibility]. Fortschr Kieferorthop (1970) 0.75