Published in Hemoglobin on January 01, 1984
Intermediary carbohydrate metabolism in embryonic life: Phosphorylation cycles. VI. Glucolysis without phosphorylation. VII. Experiments on the nature of non-phosphorylating glucolysis. Biochem J (1937) 7.09
Some factors influencing the formation of Robison ester from glycogen and inorganic phosphate in muscle extract. Biochem J (1939) 5.96
Molecular pathology of human haemoglobin. Nature (1968) 4.31
Clinical decision support systems for the practice of evidence-based medicine. J Am Med Inform Assoc (2001) 3.90
The effect of protein intake on the absorption of calcium and magnesium. Biochem J (1942) 3.02
Studies on iron in plants with special observations on the chlorophyll: iron ratio. Biochem J (1941) 2.83
[Rheumatologic treatment in the G-DRG system]. Z Rheumatol (2004) 2.58
Post-Traumatic Confusional State Treated with Massive Doses of Nicotinic Acid. Can Med Assoc J (1944) 2.54
Haemoglobin G Copenhagen and haemoglobin J Cambridge. Two new beta-chain variants of haemoglobin A. Biochim Biophys Acta (1967) 2.26
Intermediary carbohydrate metabolism in embryonic life: Glyceraldehyde and glucolysis. Biochem J (1937) 2.15
Sickling tests. Pitfalls in performance and interpretation. JAMA (1967) 2.13
Anticytoplasmic antibodies in Wegener's granulomatosis. Lancet (1986) 2.12
Variations in the structure of human haemoglobin. With particular reference to the unstable haemoglobins. Br Med Bull (1969) 2.07
Haemoglobin gene frequencies in the Jamaican population: a study in 100,000 newborns. Br J Haematol (1986) 2.00
Cation antagonism in blood coagulation. J Physiol (1944) 1.95
A distant gene deletion affects beta-globin gene function in an atypical gamma delta beta-thalassemia. J Clin Invest (1985) 1.85
Molecular evolution of myoglobin and the fossil record: a phylogenetic synthesis. Nature (1973) 1.76
Rapid estimation (2 1/2 hours) of glycosylated haemoglobin for routine purposes. Lancet (1977) 1.76
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Haemoglobin Hammersmith (beta-42 (CDI) Phe replaced by ser). Nature (1967) 1.52
Changes of trace minerals (serum iron, zinc, copper and magnesium) in thalassemia. Acta Haematol (1975) 1.47
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Abnormal haem binding and globin SH group blockade in unstable haemoglobins. Nature (1968) 1.44
Moleuclar pathology of human haemoglobin: stereochemical interpretation of abnormal oxygen affinities. Nature (1971) 1.40
A new hemoglobin variant resembling hemoglobin E. Hemoglobin E Saskatoon: beta-22 Glu replaced by Lys. Can J Biochem (1967) 1.40
[Rheumatology coding guideline. A guideline for clinical practice]. Z Rheumatol (2002) 1.40
Incidence of parvovirus B19 infection among thalassemia major patients from Ankara, Turkey. Pediatr Hematol Oncol (1996) 1.39
Human cholinesterase (pseudocholinesterase): genetic variants and their recognition. Br J Anaesth (1969) 1.35
Haemoglobin Köln (beta-98 valine--methionine): an unstable protein causing inclusion-body anaemia. Nature (1966) 1.33
Differences between alpha- and beta-chain mutants of human haemoglobin and between alpha- and beta-thalassaemia. Possible duplication of the alpha-chain gene. Br Med J (1968) 1.33
Two haemoglobins Q, alpha-74 (EF3) and alpha-75 (EF4) aspartic acid to histidine. Br J Haematol (1970) 1.28
The unstable haemoglobin haemolytic anaemias. Semin Hematol (1969) 1.27
[Structural quality of rheumatology clinics for children and adolescents. Paper by a task force of the "Society of Pediatric and Adolescent Rheumatology" and of the "Association of Rheumatology Clinics in Germany"]. Z Rheumatol (2006) 1.27
Effects of probiotic supplementation for the first 6 months of life on allergen- and vaccine-specific immune responses. Clin Exp Allergy (2006) 1.23
Haemoglobin O in An Arab Family. Br Med J (1960) 1.23
[G-DRG system 2009: relevant changes for rheumatology]. Z Rheumatol (2009) 1.22
Haemoglobin Tak: a variant with additional residues at the end of the beta-chains. Lancet (1971) 1.20
Evaluation of the effects of probiotic supplementation from the neonatal period on innate immune development in infancy. Clin Exp Allergy (2006) 1.20
[Hospital financing for 2011: relevant changes in rheumatology]. Z Rheumatol (2011) 1.15
Serum-pseudocholinesterase in depression with notable anxiety. Lancet (1965) 1.12
Seizure suppression in kindling epilepsy by grafts of fetal GABAergic neurons in rat substantia nigra. J Neurosci Res (1998) 1.11
Different types of alpha-thalassaemia and significance of haemoglobin Bart's in neonates. Lancet (1970) 1.10
A Ghanaian adult, homozygous for hereditary persistence of foetal haemoglobin and heterozygous for elliptocytosis. Acta Haematol (1970) 1.10
On the evolution of myoglobin. Philos Trans R Soc Lond B Biol Sci (1978) 1.09
Abnormal haemoglobins and the genetic code. Nature (1965) 1.08
PRE3, highly homologous to the human major histocompatibility complex-linked LMP2 (RING12) gene, codes for a yeast proteasome subunit necessary for the peptidylglutamyl-peptide hydrolyzing activity. FEBS Lett (1994) 1.06
Draft guideline on detection of toxicity to reproduction for medicinal products. Adverse Drug React Toxicol Rev (1991) 1.06
Ultrastructural findings in soft tissues adjacent to titanium plates used in jaw fracture treatment. Int J Oral Maxillofac Surg (1993) 1.05
Autoantibodies to cartilage collagens in relapsing polychondritis. Arch Dermatol Res (1993) 1.05
Haemoglobin Q India (alpha 64(E13) aspartic acid histidine) associated with beta-thalassemia observed in three Sindhi families. J Med Genet (1972) 1.05
Hereditary non-spherocytic haemolytic anaemia with post-splenectomy inclusion bodies and pigmenturia caused by an unstable haemoglobin Santa Ana-beta-88 (F4) leucine--proline. J Med Genet (1968) 1.04
Hemoglobin J Cape Town-alpha-2 92 arginine replaced by glutamine beta-2. Nature (1966) 1.04
The accuracy of haemoglobin determination by the copper sulphate-blood gravity method in indian soldiers. J Physiol (1946) 1.04
Hemoglobin Duarte: (alpha2beta2 62(E6)Ala leads to Pro): a new unstable hemoglobin with increased oxygen affinity. Blood (1974) 1.03
Haemoglobin Korle-Bu (beta 73 aspartic acid replaced by asparagine) showing one of the two amino acid substitutions of haemoglobin C Harlem. J Med Genet (1968) 1.03
The influence of steric and electronic parameters on the substrate behavior of -oxo acids to yeast pyruvate decarboxylase. Eur J Biochem (1973) 1.03
Preclinical safety testing of species-specific proteins produced with recombinant DNA-techniques. An attempt to transfer current experience into future testing strategies. Arch Toxicol (1986) 1.02
Decreased iron and zinc absorption in Turkish children with iron deficiency and geophagia. Acta Haematol (1978) 1.02
Pica in Turkey. II. Effect of clay upon iron absorption. Am J Clin Nutr (1968) 1.02
Familial occurrence of systemic vasculitis and rapidly progressive glomerulonephritis. Am J Kidney Dis (1999) 1.00
Mycoplasma crocodyli sp. nov., a new species from crocodiles. Int J Syst Bacteriol (1997) 1.00
[Hospital financing in 2012 - Relevant changes for rheumatology]. Z Rheumatol (2012) 1.00
[The G-DRG System 2009--relevant changes for rheumatology]. Z Rheumatol (2010) 0.99
A new cause of haemolytic anaemia in the newborn. A description of an unstable fetal haemoglobin: F Poole, alpha2-G-gamma2 130 trptophan yeilds glycine. J Clin Pathol (1975) 0.99
Haemoglobin sydney: Beta-67 (E11) valine modified to alanine: an emerging pattern of unstable haemoglobins. Nature (1967) 0.98
Duplication of alpha-thalassaemia gene in three Greek families with haemoglobin H disease. Lancet (1970) 0.98
A new Hb variant: Hb F Sardinia gamma75(E19) isoleucine leads to threonine found in a family with Hb G Philadelphia, beta-chain deficiency and a Lepore-like haemoglobin indistinguishable from Hb A2. Acta Haematol (1975) 0.98
Ocular granulocytic sarcoma (chloroma) with acute myelomonocytic leukemia in Turkish children. Cancer (1978) 0.98
[Quality of life and psychosocial adaptation in children and adolescents with juvenile idiopathic arthritis and reactive arthritis]. Z Rheumatol (2005) 0.97
Clinical effects of probiotics are associated with increased interferon-gamma responses in very young children with atopic dermatitis. Clin Exp Allergy (2005) 0.97
Oxygen dissociation curve of haemoglobin Portland. FEBS Lett (1975) 0.97
Haemoglobin F Texas I(alpha-2,gamma-2-5glu-lys): a variant of haemoglobin F. Br J Haematol (1967) 0.96
Familial polycythaemia caused by a new haemoglobin variant: Hb Heathrow, beta 103 (G5) phenylalanine leads to leucine. Br Med J (1973) 0.96
HD 181068: a red giant in a triply eclipsing compact hierarchical triple system. Science (2011) 0.96
Nuclear magnetic resonance studies of hemoglobins. VII. Tertiary structure around ligand binding site in carbonmonoxyhemoglobin. Biochemistry (1972) 0.96
High incidence of neural tube defects in Bursa, Turkey. Paediatr Perinat Epidemiol (1988) 0.96
Effects of weak mobile phone - electromagnetic fields (GSM, UMTS) on event related potentials and cognitive functions. Bioelectromagnetics (2008) 0.95
Alternative conceptions of memory consolidation and the role of the hippocampus at the systems level in rodents. Curr Opin Neurobiol (2011) 0.95
Haemoglobin Genova: beta-28 (B10) leucine replaced by proline. Nature (1967) 0.95
Letter: Decrease of HB-s Ag titers after repeated freezing and thawing. N Engl J Med (1975) 0.95
Atopic dermatitis in young children is associated with impaired interleukin-10 and interferon-gamma responses to allergens, vaccines and colonizing skin and gut bacteria. Clin Exp Allergy (2005) 0.94
Chlorama-like ocular manifestations in Turkish children with acute myelomonocytic leukaemia. Lancet (1971) 0.94
Some aspects of the haemoglobinopathies. Trans R Soc Trop Med Hyg (1974) 0.94
Primary portal transport of persorbed starch granules from the intestinal wall. Med Exp Int J Exp Med (1968) 0.94
The genetical interpretation of haemoglobin H disease. Hum Hered (1970) 0.94
Pica in Turkey. 1. The incidence and association with anemia. Am J Clin Nutr (1966) 0.93
Pathomorphological and biochemical alterations in Ehlers-Danlos-syndrome type IV. Pathol Res Pract (1994) 0.92
Familial sinus node dysfunction with autosomal dominant inheritance. Br Heart J (1978) 0.92
The amino acid sequence of human myoglobin and its minor fractions. Proc R Soc Lond B Biol Sci (1974) 0.92
Haemoglobin Southampton, 106 (G8) Leu leads to pro: an unstable variant producing severe haemolysis. Lancet (1972) 0.92
A double-blind, placebo-controlled dose-finding study with sertraline. Psychopharmacol Bull (1989) 0.92
Prenatal diagnosis of "dihydrobiopterin synthetase" deficiency, a variant form of phenylketonuria. Eur J Pediatr (1986) 0.92
Haemoglobin J Tongariki (alpha-115 alanine--aspartic acid): the first new haemoglobin variant found in a Pacific (Melanesian) population. J Med Genet (1967) 0.91
Haemoglobin Rahere (beta Lys-Thr): A new high affinity haemoglobin associated with decreased 2, 3-diphosphoglycerate binding and relative polycythaemia. Br Med J (1975) 0.91
Adhesion energy of receptor-mediated interaction measured by elastic deformation. Biophys J (1999) 0.91
The incidence of -thalassemia and abnormal hemoglobins in Turkey. Acta Haematol (1971) 0.91
Haemoglobin O Arab in Sudanese. Nature (1966) 0.91
Fanconi's aplastic anemia, analysis of 18 cases. Acta Haematol (1980) 0.91