AAAAAA
Results: 1-25/158
Authors:
FINCKH U
KOHLSCHUTTER A
SCHAFER H
SPERHAKE K
COLOMBO JP
GAL A
Citation: U. Finckh et al., PRENATAL-DIAGNOSIS OF CARBAMOYL-PHOSPHATE SYNTHETASE-I DEFICIENCY BY IDENTIFICATION OF A MISSENSE MUTATION IN CPS1, Human mutation, 12(3), 1998, pp. 206-211
Authors:
GAL A
ETZION O
Citation: A. Gal et O. Etzion, A MULTIAGENT UPDATE PROCESS IN A DATABASE WITH TEMPORAL DATA DEPENDENCIES AND SCHEMA VERSIONING, IEEE transactions on knowledge and data engineering, 10(1), 1998, pp. 21-37
Authors:
BUNGE S
RATHMANN M
STEGLICH C
BONDESON ML
TYLKISZYMANSKA A
POPOWSKA E
GAL A
Citation: S. Bunge et al., HOMOLOGOUS NONALLELIC RECOMBINATIONS BETWEEN THE IDURONATE-SULFATASE GENE AND PSEUDOGENE CAUSE VARIOUS INTRAGENIC DELETIONS AND INVERSIONS IN PATIENTS WITH MUCOPOLYSACCHARIDOSIS TYPE-II, European journal of human genetics, 6(5), 1998, pp. 492-500
Authors:
DENDUNNEN JT
KRAAYENBRINK T
VANSCHOONEVELD M
VANDEVOSSE E
DEJONG PTVM
TENBRINK JB
SCHUURMAN E
TIJMES N
VANOMMEN GJB
BERGEN AAB
ANDOLFI G
MONTINI E
LI Y
OUDET C
BOLZ H
KAPLAN J
ORTH U
GAL A
HANAUER A
BARDELLI AM
AYUSO C
DIAZ FJ
BITOUN P
VENTRUTO V
BALLABIO A
FRANCO B
HIRIYANNA KT
BINGHAM EL
MCHENRY C
PAWAR H
COATS C
DARGA T
RICHARDS JE
SIEVING PA
HUOPANIEMI L
RANTALA A
ROSENBERG T
DAHL N
WRIGHT A
DELACHAPELLE A
ALITALO T
LENZNER S
BRUNNER B
FEIL S
NIESLER B
SCHULZ U
PINCKERS A
BLANKENNAGEL A
RUETHER K
KELLNER U
RAPPOLD G
ROPERS HH
KALSCHEUER V
BERGER W
TRUMP D
WALPOLE SM
NICOLAOU A
GAYTHOR SA
PIMENIDES D
GEORGE NDL
MOORE UT
YATES JRW
Citation: Jt. Dendunnen et al., FUNCTIONAL IMPLICATIONS OF THE SPECTRUM OF MUTATIONS FOUND IN 234 CASES WITH X-LINKED JUVENILE RETINOSCHISIS (XLRS), Human molecular genetics (Print), 7(7), 1998, pp. 1185-1192
Authors:
FUCHSHUBER A
DELTAS CC
BERTHOLD S
STAVROU C
VOLLMER M
BURTON C
FEEST T
KRIETER D
GAL A
BRANDIS M
PIERIDES A
HILDEBRANDT F
Citation: A. Fuchshuber et al., AUTOSOMAL-DOMINANT MEDULLARY CYSTIC KIDNEY-DISEASE - EVIDENCE OF GENELOCUS HETEROGENEITY, Nephrology, dialysis, transplantation, 13(8), 1998, pp. 1955-1957
Authors:
SHEPPARD MN
LUNA R
HORIBA K
GALATEAUSALLE F
GAL A
FRANKLIN W
MILLER Y
FLEMING MV
LIOTTA LA
STATLERSTEVENSON WG
FERRANS VJ
TRAVIS WD
Citation: Mn. Sheppard et al., EXTRACELLULAR-MATRIX (ECM) REMODELING IN NEUROENDOCRINE (NEC) PROLIFERATIONS OF TH LUNG - IDIOPATHIC DIFFUSE HYPERPLASIA OF PULMONARY NEUROENDOCRINE CELLS (IDHPNEC), TUMORLETS (TL), AND CARCINOID-TUMORS (CT), Modern pathology, 11(1), 1998, pp. 179-179
Authors:
FINCKH U
XU SY
KUMARAMANICKAVEL G
SCHURMANN M
MUKKADAN JK
FERNANDEZ ST
JOHN S
WEBER JL
DENTON MJ
GAL A
Citation: U. Finckh et al., HOMOZYGOSITY MAPPING OF AUTOSOMAL RECESSIVE RETINITIS-PIGMENTOSA LOCUS (RP22) ON CHROMOSOME 16P12.1-P12.3, Genomics, 48(3), 1998, pp. 341-345
Authors:
FISHER T
BERNER T
GAL A
DUBINSKY Z
Citation: T. Fisher et al., A COMPARISON OF COMPUTERIZED IMAGE-ANALYSIS AND STEREOLOGY AS TOOLS FOR MORPHOLOGICAL-STUDY OF ALGAL CELLS, Israel journal of plant sciences, 46(2), 1998, pp. 177-180
Authors:
GAL A
Citation: A. Gal, MEDIUM EFFECTS IN K-NUCLEAR INTERACTIONS, Nuclear physics. A, 639(1-2), 1998, pp. 485-491
Authors:
GAL A
Citation: A. Gal, NUCLEAR MEDIUM EFFECTS ON K AND (K)OVER-BAR INTERACTIONS, Nuclear physics. A, 629(1-2), 1998, pp. 315-323
Authors:
FRIEDMAN E
GAL A
Citation: E. Friedman et A. Gal, ON THE DETERMINATION OF THE PION EFFECTIVE-MASS IN NUCLEI FROM PIONICATOMS, Physics letters. Section B, 432(3-4), 1998, pp. 235-240
Authors:
XU SY
ROSENBERG T
GAL A
Citation: Sy. Xu et al., REFINED GENETIC-MAPPING OF AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA LOCUS RP18 REDUCES THE CRITICAL REGION TO 2 CM BETWEEN D1S442 AND D1S2858 ON CHROMOSOME-1Q, Human genetics, 102(4), 1998, pp. 493-494
Authors:
FINCKH U
MANN U
MULLERTHOMSEN T
EGGERS C
NABER D
NITSCH RM
GAL A
Citation: U. Finckh et al., UNEXPECTED SPECTRUM OF DISEASE-CAUSING MUTATIONS IN A CLINICAL-SAMPLEOF PATIENTS WITH PRESENILE-DEMENTIA, American journal of medical genetics, 81(6), 1998, pp. 554-555
Authors:
GU SM
LENNON A
LI Y
LORENZ B
FOSSARELLO M
NORTH M
GAL A
WRIGHT A
Citation: Sm. Gu et al., TUBBY-LIKE PROTEIN-1 MUTATIONS IN AUTOSOMAL RECESSIVE RETINITIS-PIGMENTOSA, Lancet, 351(9109), 1998, pp. 1103-1104
Authors:
VORGERD M
BENKMANN HG
TEGENTHOFF M
GAL A
MALIN JP
Citation: M. Vorgerd et al., ADRENOLEUKODYSTROPHY ADRENOMYELONEUROPATH Y - CLINICAL, BIOCHEMICAL AND GENETIC FINDINGS/, Nervenarzt, 69(2), 1998, pp. 174-179
Authors:
MENKE T
GU SM
SCHLUTER B
KUWERTZBROKING E
GAL A
ANDLER W
Citation: T. Menke et al., THE LOWE-SYNDROME - CLINICAL FINDINGS AND THE DETECTION OF A GENE MUTATION IN A 4-YEAR OLD BOY, Monatsschrift fur Kinderheilkunde, 146(2), 1998, pp. 125-128
Authors:
MEINS M
KOHLHAAS M
RICHARD G
GAL A
Citation: M. Meins et al., LATTICE CORNEAL-DYSTROPHY TYPE-I - CLINIC AL AND MOLECULAR-GENETIC ANALYSIS IN A LARGE FAMILY, Klinische Monatsblatter fur Augenheilkunde, 212(3), 1998, pp. 154-158
Authors:
VESKE A
NILSSON SEG
GAL A
Citation: A. Veske et al., ORGANIZATION OF THE CANINE GENE ENCODING THE E ISOFORM OF RETINAL GUANYLATE-CYCLASE (CGC-E) AND EXCLUSION OF ITS INVOLVEMENT IN THE INHERITED RETINAL DYSTROPHY OF THE SWEDISH BRIARD AND BRIARD-BEAGLE DOGS, Biochimica et biophysica acta. Biomembranes, 1372(1), 1998, pp. 69-77
Authors:
SCHROEDER B
HESSE L
BRUCK W
GAL A
Citation: B. Schroeder et al., HISTOPATHOLOGICAL AND IMMUNOHISTOCHEMICAL FINDINGS ASSOCIATED WITH A NULL MUTATION IN THE NORRIE-DISEASE GENE, Ophthalmic genetics, 18(2), 1997, pp. 71-77
Authors:
GAL A
APFELSTEDTSYLLA E
JANECKE AR
ZRENNER E
Citation: A. Gal et al., RHODOPSIN MUTATIONS IN INHERITED RETINAL DYSTROPHIES AND DYSFUNCTIONS, Progress in retinal and eye research, 16(1), 1997, pp. 51-79
Authors:
GU SM
THOMPSON DA
SRIKUMARI CRS
LORENZ B
FINCKH U
NICOLETTI A
MURTHY KR
RATHMANN M
KUMARAMANICKAVEL G
DENTON MJ
GAL A
Citation: Sm. Gu et al., MUTATIONS IN RPE65 CAUSE AUTOSOMAL RECESSIVE CHILDHOOD-ONSET SEVERE RETINAL DYSTROPHY, Nature genetics, 17(2), 1997, pp. 194-197
Authors:
BUNGE S
INCE H
STEGLICH C
KLEIJER WJ
BECK M
ZAREMBA J
VANDIGGELEN OP
WEBER B
HOPWOOD JJ
GAL A
Citation: S. Bunge et al., IDENTIFICATION OF 16 SULFAMIDASE GENE-MUTATIONS INCLUDING THE COMMON R74C IN PATIENTS WITH MUCOPOLYSACCHARIDOSIS TYPE IIIA (SANFILIPPO-A), Human mutation, 10(6), 1997, pp. 479-485
Authors:
BUNGE S
KLEIJER WJ
TYLKISZYMANSKA A
STEGLICH C
BECK M
TOMATSU S
FUKUDA S
POORTHUIS BJHM
CZARTORYSKA B
ORII T
GAL A
Citation: S. Bunge et al., IDENTIFICATION OF 31 NOVEL MUTATIONS IN THE N-ACETYLGALACTOSAMINE-6-SULFATASE GENE REVEALS EXCESSIVE ALLELIC HETEROGENEITY AMONG PATIENTS WITH MORQUIO-A-SYNDROME, Human mutation, 10(3), 1997, pp. 223-232
Authors:
KREMMER S
ECKSTEIN A
GAL A
APFELSTEDTSYLLA E
WEDEMANN H
RUTHER K
ZRENNER E
Citation: S. Kremmer et al., OCULAR FINDINGS IN PATIENTS WITH AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA AND CYS110PHE, ARG135GLY, AND GLN344STOP MUTATIONS OF RHODOPSIN, Graefe's archive for clinical and experimental ophthalmology, 235(9), 1997, pp. 575-583
Authors:
CIEPLY A
GAL A
Citation: A. Cieply et A. Gal, CHARGE-EXCHANGE CONTRIBUTION TO PI(-4(LAMBDA) DECAY() EMISSION IN HE), Physical review. C. Nuclear physics, 55(5), 1997, pp. 2715-2718