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Results: 1-19 |
Results: 19
CLINICAL AND MOLECULAR EVALUATION OF NONDOMINANT HEREDITARY SPHEROCYTOSIS (HS)
Authors: DELGIUDICE EM NOBILI B DURZO G ILARDO R FRANCESE M CONTE ML EBER SW IOLASCON A PERROTTA S
Citation: Em. Delgiudice et al., CLINICAL AND MOLECULAR EVALUATION OF NONDOMINANT HEREDITARY SPHEROCYTOSIS (HS), British Journal of Haematology, 102(1), 1998, pp. 302-302
PSEUDONORMOTHROMBOCYTHEMIA AND PSEUDOTHROMBOCYTOSIS DUE TO RED CELL-FRAGMENTS AND TEAR DROP CELLS - A CASE FOR LOOKING AT THE BLOOD SMEAR
Authors: EBER SW SCHUTZ E KABOTH U
Citation: Sw. Eber et al., PSEUDONORMOTHROMBOCYTHEMIA AND PSEUDOTHROMBOCYTOSIS DUE TO RED CELL-FRAGMENTS AND TEAR DROP CELLS - A CASE FOR LOOKING AT THE BLOOD SMEAR, Thrombosis and haemostasis, 1997, pp. 2601-2601
MOLECULAR AND GENETIC-CHARACTERISTICS IN JAPANESE PATIENTS WITH HEREDITARY SPHEROCYTOSIS - FREQUENT BAND-3 MUTATIONS AND RARER ANKYRIN MUTATIONS
Authors: KANZAKI A TAKEZONO M KAKU M YAWATA A OZCAN R KUGLER W EBER SW YAWATA Y
Citation: A. Kanzaki et al., MOLECULAR AND GENETIC-CHARACTERISTICS IN JAPANESE PATIENTS WITH HEREDITARY SPHEROCYTOSIS - FREQUENT BAND-3 MUTATIONS AND RARER ANKYRIN MUTATIONS, Blood, 90(10), 1997, pp. 2709-2709
DETERMINATION OF GLUCOCORTICOID RECEPTOR (GR) MESSENGER-RNA LEVELS INNORMAL AND LEUKEMIC LYMPHATIC CELLS INDICATES A MATURATION DEPENDENT INCREASE
Authors: HENNIG H BOEMMER DC KUGLER W BERTRAM J SCHWINZER B WELTE K BLOBEL G EBER SW
Citation: H. Hennig et al., DETERMINATION OF GLUCOCORTICOID RECEPTOR (GR) MESSENGER-RNA LEVELS INNORMAL AND LEUKEMIC LYMPHATIC CELLS INDICATES A MATURATION DEPENDENT INCREASE, Blood, 90(10), 1997, pp. 3697-3697
PARENTAL MOSAICISM FOR ANKYRIN-1 MUTATIONS IN 2 FAMILIES WITH HEREDITARY SPHEROCYTOSIS (HS)
Authors: OZCAN R KUGLER W FEURINGBUSKE M SCHROTER W LUX SE EBER SW
Citation: R. Ozcan et al., PARENTAL MOSAICISM FOR ANKYRIN-1 MUTATIONS IN 2 FAMILIES WITH HEREDITARY SPHEROCYTOSIS (HS), Blood, 90(10), 1997, pp. 1-1
HEREDITARY PYROPOIKILOCYTOSIS (HPP) ASSOCIATED WITH A DE-NOVO ALPHA-SPECTRIN MUTATION IN CODON-28 (ARG-]HIS, SPECTRIN CORBEIL) AND LOW EXPRESSION OF THE ALPHA-SPECTRIN ALLELE IN TRANS
Authors: BOEMMER DC ULLMANN S KUGLER W DORNWELL M EBER SW GRIESINGER F
Citation: Dc. Boemmer et al., HEREDITARY PYROPOIKILOCYTOSIS (HPP) ASSOCIATED WITH A DE-NOVO ALPHA-SPECTRIN MUTATION IN CODON-28 (ARG-]HIS, SPECTRIN CORBEIL) AND LOW EXPRESSION OF THE ALPHA-SPECTRIN ALLELE IN TRANS, Blood, 90(10), 1997, pp. 4-4
ANKYRIN-1 MUTATIONS ARE A MAJOR CAUSE OF DOMINANT AND RECESSIVE HEREDITARY SPHEROCYTOSIS
Authors: EBER SW GONZALEZ JM LUX ML SCARPA AL TSE WT DORNWELL M HERBERS J KUGLER W OZCAN R PEKRUN A GALLAGHER PG SCHROTER W FORGET BG LUX SE
Citation: Sw. Eber et al., ANKYRIN-1 MUTATIONS ARE A MAJOR CAUSE OF DOMINANT AND RECESSIVE HEREDITARY SPHEROCYTOSIS, Nature genetics, 13(2), 1996, pp. 214-218
COMPLICATIONS FOLLOWING SPLENECTOMY IN BE NIGN HEMATOLOGICAL DISEASE IN CHILDREN AND ADOLESCENTS
Authors: EBER SW GROSCHE M DITZIG M PEKRUN A LAKOMEK M SCHROTER W
Citation: Sw. Eber et al., COMPLICATIONS FOLLOWING SPLENECTOMY IN BE NIGN HEMATOLOGICAL DISEASE IN CHILDREN AND ADOLESCENTS, Monatsschrift fur Kinderheilkunde, 144(3), 1996, pp. 275-280
THROMBOEMBOLIC DISEASE AFTER SPLENECTOMY FOR HEREDITARY STOMATOCYTOSIS
Authors: STEWART GW AMESS JAL EBER SW KINGSWOOD C LANE PA SMITH BD MENTZER WC
Citation: Gw. Stewart et al., THROMBOEMBOLIC DISEASE AFTER SPLENECTOMY FOR HEREDITARY STOMATOCYTOSIS, British Journal of Haematology, 93(2), 1996, pp. 303-310
PSEUDONORMOTHROMBOCYTHEMIA AND PSEUDOTHROMBOCYTOSIS DUE TO RED CELL-FRAGMENTS AND TEAR DROP CELLS - A CASE FOR LOOKING AT THE BLOOD SMEAR
Authors: EBER SW SCHUTZ E KABOTH U
Citation: Sw. Eber et al., PSEUDONORMOTHROMBOCYTHEMIA AND PSEUDOTHROMBOCYTOSIS DUE TO RED CELL-FRAGMENTS AND TEAR DROP CELLS - A CASE FOR LOOKING AT THE BLOOD SMEAR, Blood, 88(10), 1996, pp. 2963-2963
SPECTRIN ALPHA-ESCHE, A NOVEL TRUNCATED SPECTRIN ALPHA-CHAIN VARIANT DUE TO SKIPPING OF EXON-39, LEADING TO SEVERE INFANTILE POIKILOCYTOSIS
Authors: ULLMANN S KUGLER W DORNWELL M AHLE S BOMMER DC SCHROTER W GALLAGHER P FORGET B EBER SW
Citation: S. Ullmann et al., SPECTRIN ALPHA-ESCHE, A NOVEL TRUNCATED SPECTRIN ALPHA-CHAIN VARIANT DUE TO SKIPPING OF EXON-39, LEADING TO SEVERE INFANTILE POIKILOCYTOSIS, Blood, 88(10), 1996, pp. 5-5
HIGH-FREQUENCY OF FRAMESHIFT NONSENSE MUTATIONS OF ANKYRIN-1 IN CZECHPATIENTS WITH DOMINANT HEREDITARY SPHEROCYTOSIS (DHS)/
Authors: OZCAN R JAROLIM P BRABEC V LUX SE EBER SW
Citation: R. Ozcan et al., HIGH-FREQUENCY OF FRAMESHIFT NONSENSE MUTATIONS OF ANKYRIN-1 IN CZECHPATIENTS WITH DOMINANT HEREDITARY SPHEROCYTOSIS (DHS)/, Blood, 88(10), 1996, pp. 10-10
TRIOSEPHOSPHATE ISOMERASE DEFICIENCY - BIOCHEMICAL AND MOLECULAR-GENETIC ANALYSIS FOR PRENATAL-DIAGNOSIS
Authors: PEKRUN A NEUBAUER BA EBER SW LAKOMEK M SEIDEL H SCHROTER W
Citation: A. Pekrun et al., TRIOSEPHOSPHATE ISOMERASE DEFICIENCY - BIOCHEMICAL AND MOLECULAR-GENETIC ANALYSIS FOR PRENATAL-DIAGNOSIS, Clinical genetics, 47(4), 1995, pp. 175-179
INVESTIGATIONS OF 14-ANKYRIN POLYMORPHISMS EXCLUDE LARGE DELETIONS OFTHE ANKYRIN GENE AS A MAJOR CAUSE OF HEREDITARY SPHEROCYTOSIS
Authors: EBER SW GONZALEZ JM LUX ML GALLAGHER PG FORGET BG LUX SE
Citation: Sw. Eber et al., INVESTIGATIONS OF 14-ANKYRIN POLYMORPHISMS EXCLUDE LARGE DELETIONS OFTHE ANKYRIN GENE AS A MAJOR CAUSE OF HEREDITARY SPHEROCYTOSIS, Blood, 84(10), 1994, pp. 10000008-10000008
HEREDITARY SPHEROCYTOSIS WITH ANKYRIN WALSRODE, A VARIANT ANKYRIN WITH DECREASED AFFINITY FOR BAND-3
Authors: EBER SW PEKRUN A REINHARDT D SCHROTER W LUX SE
Citation: Sw. Eber et al., HEREDITARY SPHEROCYTOSIS WITH ANKYRIN WALSRODE, A VARIANT ANKYRIN WITH DECREASED AFFINITY FOR BAND-3, Blood, 84(10), 1994, pp. 10000362-10000362
REGULATION OF BAND 3 ROTATIONAL MOBILITY BY ANKYRIN IN INTACT HUMAN RED-CELLS
Authors: CHO MR EBER SW LUX SE GOLAN DE
Citation: Mr. Cho et al., REGULATION OF BAND 3 ROTATIONAL MOBILITY BY ANKYRIN IN INTACT HUMAN RED-CELLS, Biophysical journal, 66(2), 1994, pp. 10000067-10000067
COMBINED ANKYRIN AND SPECTRIN DEFICIENCY IN HEREDITARY SPHEROCYTOSIS
Authors: PEKRUN A EBER SW KUHLMEY A SCHROTER W
Citation: A. Pekrun et al., COMBINED ANKYRIN AND SPECTRIN DEFICIENCY IN HEREDITARY SPHEROCYTOSIS, Annals of hematology, 67(2), 1993, pp. 89-93
INCREASED BAND 3 MOBILITY AND DECREASED ANION TRANSPORT IN ANKYRIN DEFICIENT HEREDITARY SPHEROCYTES
Authors: EBER SW CHO M BRUGNARA C MOHANDAS N GOLAN DE PEKRUN A DORNWELL M HANSPAL M LIU SC CHILCOTE R PALEK J FORGET BG LUX SE
Citation: Sw. Eber et al., INCREASED BAND 3 MOBILITY AND DECREASED ANION TRANSPORT IN ANKYRIN DEFICIENT HEREDITARY SPHEROCYTES, Blood, 82(10), 1993, pp. 10000175-10000175
DISCOVERY OF 8 ANKYRIN MUTATIONS IN HEREDITARY SPHEROCYTOSIS (HS) INDICATES THAT ANKYRIN DEFECTS ARE A MAJOR CAUSE OF DOMINANT AND RECESSIVE HS
Authors: EBER SW LUX ML GONZALEZ JM SCARPA A TSE WT GALLAGHER PG PEKRUN A FORGET BG LUX SE
Citation: Sw. Eber et al., DISCOVERY OF 8 ANKYRIN MUTATIONS IN HEREDITARY SPHEROCYTOSIS (HS) INDICATES THAT ANKYRIN DEFECTS ARE A MAJOR CAUSE OF DOMINANT AND RECESSIVE HS, Blood, 82(10), 1993, pp. 10000308-10000308
Risultati: 1-19 |