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Results: 1-9 |
Results: 9
FUNCTIONAL-ACTIVITY OF CD44 ISOFORMS IN HEMATOPOIESIS OF THE RAT
Authors: KHALDOYANIDI S SCHNABEL D FOHR N ZOLLER M
Citation: S. Khaldoyanidi et al., FUNCTIONAL-ACTIVITY OF CD44 ISOFORMS IN HEMATOPOIESIS OF THE RAT, British Journal of Haematology, 96(1), 1997, pp. 31-45
SEVERE HYPOKALEMIA DUE TO HYPERRENINAEMIA AND SECONDARY HYPERALDOSTERONISM IN A BOY WITH PHEOCHROMOCYTOMA
Authors: GOPEL W SCHNABEL D VOLGER S GRUTERS A
Citation: W. Gopel et al., SEVERE HYPOKALEMIA DUE TO HYPERRENINAEMIA AND SECONDARY HYPERALDOSTERONISM IN A BOY WITH PHEOCHROMOCYTOMA, European journal of pediatrics, 155(2), 1996, pp. 147-148
PHENOTYPIC CLASSIFICATION OF MALE PSEUDOHERMAPHRODITISM DUE TO STEROID 5-ALPHA-REDUCTASE-2 DEFICIENCY
Authors: SINNECKER GHG HIORT O DIBBELT L ALBERS N DORR HG HAUSS H HEINRICH U HEMMINGHAUS M HOEPFFNER W HOLDER M SCHNABEL D KRUSE K
Citation: Ghg. Sinnecker et al., PHENOTYPIC CLASSIFICATION OF MALE PSEUDOHERMAPHRODITISM DUE TO STEROID 5-ALPHA-REDUCTASE-2 DEFICIENCY, American journal of medical genetics, 63(1), 1996, pp. 223-230
TRANSIENT CONGENITAL HYPOTHYROIDISM AND HYPERTHYROTROPINEMIA - NORMALTHYROID-FUNCTION AND PHYSICAL DEVELOPMENT AT THE AGES OF 6-14 YEARS
Authors: KOHLER B SCHNABEL D BIEBERMANN H GRUTERS A
Citation: B. Kohler et al., TRANSIENT CONGENITAL HYPOTHYROIDISM AND HYPERTHYROTROPINEMIA - NORMALTHYROID-FUNCTION AND PHYSICAL DEVELOPMENT AT THE AGES OF 6-14 YEARS, The Journal of clinical endocrinology and metabolism, 81(4), 1996, pp. 1563-1567
MOLECULAR-CLONING AND CHARACTERIZATION OF A FULL-LENGTH COMPLEMENTARY-DNA ENCODING HUMAN ACID CERAMIDASE - IDENTIFICATION OF THE FIRST MOLECULAR LESION CAUSING FARBER-DISEASE
Authors: KOCH J GARTNER S LI CM QUINTERN LE BERNARDO K LEVRAN O SCHNABEL D DESNICK RJ SCHUCHMAN EH SANDHOFF K
Citation: J. Koch et al., MOLECULAR-CLONING AND CHARACTERIZATION OF A FULL-LENGTH COMPLEMENTARY-DNA ENCODING HUMAN ACID CERAMIDASE - IDENTIFICATION OF THE FIRST MOLECULAR LESION CAUSING FARBER-DISEASE, The Journal of biological chemistry, 271(51), 1996, pp. 33110-33115
INFLUENCE OF PASSIVE SMOKING ON LUNG-FUNC TION IN CHILDREN AND ADULTS
Authors: SCHNABEL D SYBRECHT GW
Citation: D. Schnabel et Gw. Sybrecht, INFLUENCE OF PASSIVE SMOKING ON LUNG-FUNC TION IN CHILDREN AND ADULTS, Medizinische Klinik, 90(7), 1995, pp. 423-427
URINARY-EXCRETION OF GALACTOSYL-HYDROXYLYSINE IS A MARKER OF GROWTH IN CHILDREN
Authors: RAUCH F SCHNABEL D SEIBEL MJ REMER T STABREY A MICHALK D SCHONAU E
Citation: F. Rauch et al., URINARY-EXCRETION OF GALACTOSYL-HYDROXYLYSINE IS A MARKER OF GROWTH IN CHILDREN, The Journal of clinical endocrinology and metabolism, 80(4), 1995, pp. 1295-1300
DETECTION OF POINT MUTATIONS IN THE ANDROGEN RECEPTOR GENE USING NONISOTOPIC SINGLE-STRAND CONFORMATION POLYMORPHISM ANALYSIS
Authors: HIORT O WODTKE A STRUVE D ZOLLNER A SINNECKER GHG ALBERS N BEYE M BEYER P BIRR C BLUNCK W BRACK C BRAMSWIG J DORR HG GAL A HECKER W HEIDEMANN P HEINRICH U HEISE HR HESSE V HINKEL M HOEPFFNER W HOLDER M KEIM L KLASEN M KORSCH E KRUGER G LANDENDORFER W MIX M MORLOT M MUHLENBERG R OTTEN A PARTSCH CJ PELZ L VONPETRYKOWSKI W RABL W REICH H SCHENK B SCHNABEL D SIPPELL W
Citation: O. Hiort et al., DETECTION OF POINT MUTATIONS IN THE ANDROGEN RECEPTOR GENE USING NONISOTOPIC SINGLE-STRAND CONFORMATION POLYMORPHISM ANALYSIS, Human molecular genetics, 3(7), 1994, pp. 1163-1166
MOLECULAR-GENETICS OF GM2-GANGLIOSIDOSIS AB-VARIANT - A NOVEL MUTATION AND EXPRESSION IN BHK CELLS
Authors: SCHRODER M SCHNABEL D HURWITZ R YOUNG E SUZUKI K SANDHOFF K
Citation: M. Schroder et al., MOLECULAR-GENETICS OF GM2-GANGLIOSIDOSIS AB-VARIANT - A NOVEL MUTATION AND EXPRESSION IN BHK CELLS, Human genetics, 92(5), 1993, pp. 437-440
Risultati: 1-9 |