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Citation: V. Martel et al., ISOLATION AND GENOMIC CHARACTERIZATION OF FETAL CELLS IN MATERNAL BLOOD USING MICRODISSECTION AND PCR, European journal of human genetics, 6, 1998, pp. 4189-4189
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SCHMIDTROSE T
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Citation: C. Kubisch et al., CLC-1 CHLORIDE CHANNEL MUTATIONS IN MYOTONIA-CONGENITA - VARIABLE PENETRANCE OF MUTATIONS SHIFTING THE VOLTAGE-DEPENDENCE, Human molecular genetics (Print), 7(11), 1998, pp. 1753-1760
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Citation: O. Uteza et al., INFLUENCE OF CATHODE ROUGHNESS ON DISCHARGE HOMOGENEITY OF A HIGH-PULSE REPETITION FREQUENCY LONG-PULSE XECL LASER, Applied physics. B, Lasers and optics, 67(2), 1998, pp. 185-191
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Citation: O. Uteza et al., IMPROVEMENT OF AVERAGE LASER POWER AND BEAM DIVERGENCE OF A HIGH PULSE REPETITION FREQUENCY EXCIMER-LASER, Applied physics. B, Lasers and optics, 66(1), 1998, pp. 31-37
Citation: B. Fontaine et al., EVOLUTION OF THE RELATIONSHIP BETWEEN NEAR GLOBAL AND ATLANTIC SST MODES AND THE RAINY-SEASON IN WEST-AFRICA - STATISTICAL-ANALYSES AND SENSITIVITY EXPERIMENTS, Climate dynamics, 14(5), 1998, pp. 353-368
Citation: S. Janicot et al., WEST-AFRICAN MONSOON DYNAMICS AND EASTERN EQUATORIAL ATLANTIC AND PACIFIC SST ANOMALIES (1970-88), Journal of climate, 11(8), 1998, pp. 1874-1882
Citation: L. Almanza et al., 4 HOURS FOR A RECORD, OR A REALLY FULMINA TING CELLULITIS - CAN SACCHAROMYCES-CEREVISIAE BE THE CAUSAL AGENT, Annales francaises d'anesthesie et de reanimation, 17(2), 1998, pp. 130-132
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Citation: G. Casari et al., SPASTIC PARAPLEGIA AND OXPHOS IMPAIRMENT CAUSED BY MUTATIONS IN PARAPLEGIN, A NUCLEAR-ENCODED MITOCHONDRIAL METALLOPROTEASE, Cell, 93(6), 1998, pp. 973-983
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Citation: H. Hosseini et al., ATAXIA AS THE FIRST SIGN OF PERNICIOUS-ANEMIA ASSOCIATED WITH AUTOIMMUNE POLYENDOCRINOPATHY, Revue neurologique, 154(10), 1998, pp. 706-707
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Citation: C. Mertens et al., A SYSTEMATIC STUDY OF OLIGODENDROCYTE GROWTH-FACTORS AS CANDIDATES FOR GENETIC SUSCEPTIBILITY TO MS, Neurology, 51(3), 1998, pp. 748-753
Authors:
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Citation: E. Plassartschiess et al., NOVEL MUSCLE CHLORIDE CHANNEL (CLCN1) MUTATIONS IN MYOTONIA-CONGENITAWITH VARIOUS MODES OF INHERITANCE INCLUDING INCOMPLETE DOMINANCE AND PENETRANCE, Neurology, 50(4), 1998, pp. 1176-1179
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Citation: O. Gaillard et al., APOLIPOPROTEIN-E AND MULTIPLE-SCLEROSIS - A BIOCHEMICAL AND GENETIC INVESTIGATION, Journal of the neurological sciences, 158(2), 1998, pp. 180-186
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Citation: I. Sipos et al., SKELETAL-MUSCLE DHP RECEPTOR MUTATIONS ALTER CALCIUM CURRENTS IN HUMAN HYPOKALEMIC PERIODIC PARALYSIS MYOTUBES (VOL 483, PG 299, 1995), Journal of physiology, 508(3), 1998, pp. 955-955
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Citation: E. Plassartschiess et al., FUNCTIONAL EXPRESSION OF THE ILE693THR NA-CONGENITA IN A HUMAN CELL-LINE( CHANNEL MUTATION ASSOCIATED WITH PARAMYOTONIA), Journal of physiology, 507(3), 1998, pp. 721-727
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Citation: K. Jurkatrott et al., CALCIUM CURRENTS AND TRANSIENTS OF NATIVE AND HETEROLOGOUSLY EXPRESSED MUTANT SKELETAL-MUSCLE DHP RECEPTOR ALPHA-1 SUBUNITS (R528H), FEBS letters, 423(2), 1998, pp. 198-204
Authors:
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Citation: A. Tourbah et al., SYSTEMIC AUTOIMMUNE FEATURES AND MULTIPLE-SCLEROSIS - A 5-YEAR FOLLOW-UP-STUDY, Archives of neurology, 55(4), 1998, pp. 517-521
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CARLIOZ R
FONTAINE B
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JANCOVICI R
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Citation: P. Brandstatt et al., POSTTRAUMATIC ACUTE AORTIC-VALVE INCOMPETENCE - ROLE OF TRANSESOPHAGEAL ECHOCARDIOGRAPHY IN DIAGNOSIS OF THE LESIONS AND TREATMENT, Annales de cardiologie et d'angeiologie, 47(8), 1998, pp. 563-567