PubRank

E Kohne

Author PubWeight™ 39.59‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Identification of new prognosis factors from the clinical and epidemiologic analysis of a registry of 229 Diamond-Blackfan anemia patients. DBA group of Société d'Hématologie et d'Immunologie Pédiatrique (SHIP), Gesellshaft für Pädiatrische Onkologie und Hämatologie (GPOH), and the European Society for Pediatric Hematology and Immunology (ESPHI). Pediatr Res 1999 2.16
2 Anaemia in pregnant Ghanaian women: importance of malaria, iron deficiency, and haemoglobinopathies. Trans R Soc Trop Med Hyg 2000 1.23
3 Thalassemia intermedia: moderate reduction of beta globin gene transcriptional activity by a novel mutation of the proximal CACCC promoter element. Blood 1991 1.20
4 Treatment with hydroxyurea in thalassemia intermedia with paravertebral pseudotumors of extramedullary hematopoiesis. Ann Hematol 2002 1.14
5 Diagnosis of diabetes in cystic fibrosis and thalassemia major. Diabetes Care 1998 1.10
6 The proximal element of the beta globin locus control region is not functionally required in vivo. J Clin Invest 1991 1.03
7 Epidemiological situation and treatment of patients with thalassemia major in Germany: results of the German multicenter beta-thalassemia study. Ann Hematol 2000 1.01
8 [Psychosocial aspects of beta-thalassemia: distress, coping and adherence]. Klin Padiatr 2000 1.00
9 Beta-thalassaemia in the immigrant and non-immigrant German populations. Br J Haematol 1997 0.94
10 Haemoglobinopathies and newborn haemoglobinopathy screening in Germany. J Clin Pathol 2009 0.92
11 Recent developments in iron chelation therapy. Klin Padiatr 2007 0.89
12 The excretion of diamines in human urine. II. Cadaverine, putrescine, 1,3-diaminopropane, 2,2'-dithiobis(ethylamine) and spermidine in urine of patients with cystinuria and cystinlysinuria. Clin Chim Acta 1971 0.87
13 A deletion/inversion rearrangement of the beta-globin gene cluster in a Turkish family with delta beta zero-thalassemia intermedia. Blood 1992 0.85
14 DNA-polymorphic patterns linked to the beta-globin genes in German families affected with hemoglobinopathies and thalassemias: a comparison to other ethnic groups. Hum Genet 1985 0.85
15 Dominant beta-thalassaemia: a highly unstable haemoglobin is caused by a novel 6 bp deletion of the beta-globin gene. Br J Haematol 2000 0.83
16 Analysis of the Hb M Milwaukee mutation at the DNA level. Br J Haematol 1983 0.83
17 A microdeletion syndrome due to a 3-Mb deletion on 19q13.2--Diamond-Blackfan anemia associated with macrocephaly, hypotonia, and psychomotor retardation. Clin Genet 1999 0.83
18 Cardiac and extracardiac complications in infants of diabetic mothers and their relation to parameters of carbohydrate metabolism. Eur J Pediatr 1997 0.83
19 Rapid and non-radioactive prenatal diagnosis of beta thalassaemia and sickle cell disease: application of the polymerase chain reaction (PCR). Br J Haematol 1988 0.82
20 [Beta-thalassemia in Germany. Results of cooperative beta-thalassemia study]. Klin Padiatr 2000 0.82
21 Hemoglobinopathy York [beta146 (HC3) His==>Pro]: first report of a family history. Ann Hematol 2001 0.82
22 Anaemia, thrombocytopenia and coagulopathy due to occult diffuse infantile haemangiomatosis of spleen and pancreas. Eur J Pediatr 1999 0.82
23 [Electrophoretic demonstration of normal and abnormal hemoglobins. Screening program using cellulose-acetate membranes]. Fortschr Med 1973 0.82
24 Persistent cyanosis in a 4 month old infant with severe pneumonia and haemoglobin M. Klin Padiatr 2009 0.82
25 [Occureence and heterogeneity of abnormal haemoglobins and thalassemia syndromes in the German population (author's transl)]. Klin Wochenschr 1974 0.82
26 [Etiology of the Calvé-Legg Perthes syndrome. Hematologic, genetic and histologic studies]. Munch Med Wochenschr 1971 0.81
27 Sickle cell-beta +-thalassaemia: a haematological and clinical study in Liberia. Blut 1983 0.81
28 Hemoglobin Presbyterian [beta 108 (G10) Asn replaced by Lys] in a German family. Hemoglobin 1979 0.81
29 Hemoglobin A1c (HbA1c) in children with long standing and newly diagnosed diabetes mellitus. Acta Paediatr Scand 1979 0.80
30 [Treatment of aplastic anemia--aims and development of the SAA 94 pilot protocol]. Klin Padiatr 1994 0.79
31 Hemoglobin M Iwate is caused by a C----T transition in codon 87 of the human alpha 1-globin gene. Hum Genet 1987 0.79
32 Hereditary hyperferritinemia cataract syndrome: clinical, genetic, and laboratory findings in 5 families. Klin Padiatr 2011 0.78
33 Cyclophosphamide cardiotoxicity. Eur J Pediatr 1980 0.78
34 Transplacental passage of foetal blood cells. Scand J Haematol 1975 0.78
35 Allogeneic bone marrow transplantation in conventional mice: I. Effect of antibiotic therapy on long term survival of allogeneic chimeras. Blut 1977 0.78
36 [Monitoring pregnant patients from risk countries with sickle cell disease and thalassemia. Clinical aspects, screening and prenatal diagnosis]. Geburtshilfe Frauenheilkd 1993 0.77
37 [Correlation between maternal hemoglobin levels and placental morphology and findings in newborn infants]. Z Geburtshilfe Perinatol 1987 0.77
38 IgG therapy in systemic lupus erythematosus--two case reports. Blut 1984 0.77
39 Heterogeneity of the alpha-globin gene defects in German alpha-thalassemia affected families. Hum Genet 1985 0.77
40 Genetic studies in Saudi Arabia: red cell enzyme, haemoglobin and serum protein polymorphisms. Am J Phys Anthropol 1979 0.77
41 [Hemoglobin D Punjab in a German patient]. Verh Dtsch Ges Inn Med 1972 0.76
42 [Hb Tübingen. A new beta-chain variant (beta Tp 10-21) with increased spontaneous oxidation]. Klin Wochenschr 1971 0.76
43 CD95 (APO-1/FAS)-mediated apoptosis in cytokine-activated hematopoietic cells. Exp Hematol 1998 0.76
44 Free alpha chains in adult and cord blood haemolysates. I. Quantitative data and identification. Res Exp Med (Berl) 1973 0.75
45 Therapy of acute lymphocytic leukemia in childhood with intermediate dose methotrexate and CNS irradiation. A report of the ALL 77-02 study group. Blut 1983 0.75
46 [The Munich study on the treatment of acute lymphoblastic leukemia in childhood (ALL 77-02)]. Klin Padiatr 1985 0.75
47 Beta-thalassemia problems in the Turkish population in the F.R.G. Eur J Obstet Gynecol Reprod Biol 1990 0.75
48 Donor cell leukemia after bone marrow transplantation in the Friend leukemia in mice. Transplantation 1980 0.75
49 [Erythrocyte hypocromia in heterozygous hemoglobin E (beta 26 Glu replaced by Lys)]. Acta Haematol 1976 0.75
50 [Human hemoglobins: normal, abnormal and pathological variants]. Internist (Berl) 1978 0.75
51 Glucose intolerance in patients with thalassemia major: insulin resistance and hyperproinsulinemia. J Pediatr Endocrinol Metab 1998 0.75
52 Hemoglobin F Koelliker (alpha2 minus 141 (HC 3) Arg gamma2); a modification of fetal hemoglobin. Hemoglobin 1977 0.75
53 Hb M Milwaukee in a German family. Hemoglobin 1977 0.75
54 Hb M Milwaukee: direct detection of the beta-globin gene mutation in three generations of an afflicted family. Hum Genet 1983 0.75
55 [The 10-minute consultation: anemia as a chance finding]. MMW Fortschr Med 2004 0.75
56 Haemoglobin D-beta-thalassaemia in a German family. A double heterozygous haemoglobinopathy. Klin Wochenschr 1985 0.75
57 The effect of irradiated blood mononuclear cells on the hemoglobin biosynthesis in cultures of erythroid progenitors from adults and neonates. Hemoglobin 1987 0.75
58 [Treatment of Crohn disease with intravenous immunoglobulin]. Monatsschr Kinderheilkd 1988 0.75
59 [Excretion of diamines in human urine. I. Excretion of di- and polyamines in urine of healthy persons of various age groups, in urine of patients with cystinuria, cystinelysinuria and enteropathy, malabsorption, enteritis and vitamin D deficiency rickets]. Klin Wochenschr 1969 0.75
60 [Heinz body formation in red cells of newborn infants. II. Clinical observations on methylene-blue-induced hemolytic Heinz body anemia (author's transl)]. Monatsschr Kinderheilkd 1974 0.75
61 [Congenital hemolytic Heinz body anemia with instable hemoglobins]. Monatsschr Kinderheilkd 1976 0.75
62 Haemoglobin A1c: a predictor for the duration of the remission phase in juvenile insulin-dependent diabetic patients. Acta Paediatr Scand 1980 0.75
63 Thalassemia intermedia: compound heterozygous beta zero/beta(+)-thalassemia and co-inherited heterozygous alpha(+)-thalassemia. Ann Hematol 1993 0.75
64 [Diseases of the hematological cell systems. 1. Diseases of the red blood cells]. Kinderkrankenschwester 1990 0.75
65 [Dysfunction of Granulocytes in Children with Frequent Infections]. Monatsschr Kinderheilkd 1976 0.75
66 [Thalassemia minor in German families on the left bank of the middle Rhine]. Med Welt 1975 0.75
67 [Enterogenous toxic methemoglobinemia in babies with severe enteritis as a result of cow's milk intolerance (author's transl)]. Klin Padiatr 1974 0.75
68 [HbM Erlangen: alpha2beta263(e7) tyr. New mutation with haemolysis and NADH-methaemoglobin reductase deficiency (author's transl)]. Z Kinderheilkd 1975 0.75
69 [Incidence and symptoms of cow's milk protein intolerance following acute gastroenteritis in young infants. Effect of a hypoallergenic diet]. Monatsschr Kinderheilkd 1989 0.75
70 [Oxygen transport function of the blood in hereditary methemoglobinemia. Role of 2,3-diphosphoglycerate]. Monatsschr Kinderheilkd 1973 0.75
71 [Beta thalassemia in Germany: molecular genetics and clinical phenotype in immigrant and in the native population]. Klin Padiatr 1997 0.75
72 Hyperphenylalaninemia caused by dihydropteridine reductase deficiency in children receiving chemotherapy for acute lymphoblastic leukemia. J Pediatr 1989 0.75
73 [Megaloblastic anaemia in childhood due to vitamin B12 deficiency, report of 3 cases of congenital selective vitamin B12 malabsorption (author's tranls)]. Klin Padiatr 1976 0.75
74 [Toxic hemolytic anemias]. Blut 1976 0.75
75 Silastic catheters for home antibiotic therapy in patients with cystic fibrosis. Eur J Pediatr 1997 0.75
76 [Bone marrow transplantation in panmyelopathy, acute leukemia and chronic myelocytic leukemia: results of the Ulm Transplantation Group]. Klin Wochenschr 1984 0.75
77 [Experiences with Pimafucin in candida and trichomonas vaginitis]. Med Welt 1969 0.75
78 [The diagnostic importance of the determination of fetal hemoglobin]. Hamatol Bluttransfus 1972 0.75
79 [Haemolysis as initial sign of Clostridium perfringens septicaemia in newborn (author's transl)]. Klin Padiatr 1981 0.75
80 Congenital erythrocytosis and polycythemia vera in childhood and adolescence. Klin Padiatr 2004 0.75
81 [Familial polyglobulism--a rare differential diagnosis of polycythemia vera]. Med Klin (Munich) 1988 0.75
82 [Hemoglobinopathies and drugs]. Haematol Blood Transfus 1978 0.75
83 [Malignant hyperthermia. 2 unusual courses]. Intensivmed Prax 1980 0.75
84 [Diagnosis of thalassemias]. Monatsschr Kinderheilkd 1979 0.75
85 [Heinz body formation in erythrocytes of the newborn. I. In vitro studies on experimental conditions and on the effect of exchange transfusions]. Acta Haematol 1970 0.75
86 [Hemolytic diseases of the newborn infant]. Monatsschr Kinderheilkd 1979 0.75
87 Hemoglobin Köln: direct analysis of the gene mutation by synthetic DNA probes. Blood 1986 0.75
88 [Diagnosis of abnormal hemoglobins]. Monatsschr Kinderheilkd 1980 0.75
89 [A simple method of haemoglobin chain dissociation by microzone electrophoresis]. Clin Chim Acta 1972 0.75
90 Structural and functional characteristics of Hb Tübingen: beta 106 (G 8) Leu leads to Gln. FEBS Lett 1976 0.75
91 Alpha-globin gene deletion causes alpha-thalassemia syndromes in two German families. Hum Genet 1984 0.75
92 [The molecular basis of hereditary persistence of fetal hemoglobin (HPFH). Clinical importance of the hemoglobin switching mechanism with special reference to Corfu delta beta zero thalassemia]. Monatsschr Kinderheilkd 1988 0.75
93 Hemoglobin Köln: analysis of linkage relationships between the mutant gene and polymorphic restriction sites in the beta-globin gene cluster. Blut 1984 0.75
94 Relation between the degree of initial metabolic decompensation and the duration of the remission phase in type I diabetes mellitus. Eur J Pediatr 1982 0.75
95 [Diseases of the hematologic cell systems. 2. Diseases of the white blood cells]. Kinderkrankenschwester 1990 0.75
96 [Neonatal polycythaemia and haemoglobin types in infants with G-trisomy (author's transl)]. Klin Wochenschr 1975 0.75
97 Haemoglobin Freiburg: direct detection by synthetic oligonucleotide probes. Hum Genet 1988 0.75
98 DNA restriction mapping identifies the chromosome carrying the mutant Hb Presbyterian beta-globin gene. Hum Genet 1983 0.75
99 Congenital stomatocytosis and chronic haemolytic anaemia. Scand J Haematol 1975 0.75
100 [Treatment of Fanconi anemia by bone marrow transplantation]. Monatsschr Kinderheilkd 1987 0.75
101 [An unusual etiology of erythrocytosis in a 23-year-old primiparous woman in the 22nd week of pregnancy]. Med Klin (Munich) 2001 0.75