au.\*:("GAL, Andreas")
Results 1 to 25 of 54
Selection :
Java Bytecode Verification via Static Single Assignment FormGAL, Andreas; PROBST, Christian W; FRANZ, Michael et al.ACM transactions on programming languages and systems. 2008, Vol 30, Num 4, issn 0164-0925, 21.1-21.21Article
Toward a consensus in the laboratory diagnostics of Fabry disease - recommendations of a European expert groupGAL, Andreas; HUGHES, Derralynn A; WINCHESTER, Bryan et al.Journal of inherited metabolic disease. 2011, Vol 34, Num 2, pp 509-514, issn 0141-8955, 6 p.Article
A novel 9 bp deletion in the Filamin A gene causes an otopalatodigital-spectrum disorder with a variable, intermediate phenotypeSTEFANOVA, Margarita; MEINECKE, Peter; GAL, Andreas et al.American journal of medical genetics. 2005, Vol 132A, Num 4, pp 386-390, issn 0148-7299, 5 p.Article
Interaction of αPIX (ARHGEF6) with β-parvin (PARVB) suggests an involvement of αPIX in integrin-mediated signalingROSENBERGER, Georg; JANTKE, Inka; GAL, Andreas et al.Human molecular genetics (Print). 2003, Vol 12, Num 2, pp 155-167, issn 0964-6906, 13 p.Article
Object-Orientation and Operating SystemsGAL, Andreas; SPINCZYK, Olaf; ALVAREZ, Dario et al.Lecture notes in computer science. 2002, pp 174-183, issn 0302-9743, isbn 3-540-00233-2, 10 p.Conference Paper
Sensory neuropathy with bone destruction due to a mutation in the membrane-shaping atlastin GTPase 3KORNAK, Uwe; MADEMAN, Inès; POU-SERRADELL, Adolf et al.Brain. 2014, Vol 137, pp 683-692, issn 0006-8950, 10 p., 3Article
Female carriers of X-chromosomal adrenoleukodystrophy: a major differential diagnosis in progressive myelopathyGUETTSCHES, Anne-Katrin; KUECHLER, Alma; GAL, Andreas et al.Journal of neurology. 2010, Vol 257, Num 8, pp 1394-1395, issn 0340-5354, 2 p.Article
Mucopolysaccharidosis type II in females : Case report and review of literatureTUSCHL, Karin; GAL, Andreas; PASCHKE, Eduard et al.Pediatric neurology. 2005, Vol 32, Num 4, pp 270-272, issn 0887-8994, 3 p.Article
Familiäre Foveahypoplasie: Klinische Einordnung = Hereditary foveal hypoplasia: Clinical differentiationSCHROEDER, Hans Wolfgang; ORTH, Ulrike; MEYER-KÖNIG, Eberhard et al.Klinische Monatsblätter für Augenheilkunde. 2003, Vol 220, Num 8, pp 559-562, issn 0023-2165, 4 p.Article
The early clinical phenotype of Fabry disease: a study on 35 European children and adolescentsRIES, Markus; RAMASWAMI, Uma; PARINI, Rossella et al.European journal of pediatrics. 2003, Vol 162, Num 11, pp 767-772, issn 0340-6199, 6 p.Article
No association between DCP1 genotype and late-onset Alzheimer diseaseBUSS, Svenja; MÜLLER-THOMSEN, Tomas; HOCK, Cristoph et al.American journal of medical genetics. 2002, Vol 114, Num 4, pp 440-445, issn 0148-7299Article
Mutations in ARHGEF6, encoding a guanine nucleotide exchange factor for Rho GTPases, in patients with X-linked mental retardationKUTSCHE, Kerstin; YNTEMA, Helger; MORAINE, Claude et al.Nature genetics. 2000, Vol 26, Num 2, pp 247-250, issn 1061-4036Article
Compartmental Memory Management in a Modern Web BrowserWAGNER, Gregor; GAL, Andreas; WIMMER, Christian et al.ACM SIGPLAN notices. 2011, Vol 46, Num 11, pp 119-128, issn 1523-2867, 10 p.Article
A high-throughput resequencing microarray for autosomal dominant spastic paraplegia genesDUFKE, Claudia; SCHLIPF, Nina; KLOPSTOCK, Thomas et al.Neurogenetics (Oxford. Print). 2012, Vol 13, Num 3, pp 215-227, issn 1364-6745, 13 p.Article
Onset and progression of the Anderson-Fabry disease related cardiomyopathyKAMPMANN, Christoph; LINHART, Ales; BAEHNER, Frank et al.International journal of cardiology. 2008, Vol 130, Num 3, pp 367-373, issn 0167-5273, 7 p.Article
The phenotype of early-onset retinal degeneration in persons with RDH12 mutationsSCHUSTER, Andreas; JANECKE, Andreas R; WILKE, Robert et al.Investigative ophthalmology & visual science. 2007, Vol 48, Num 4, pp 1824-1831, issn 0146-0404, 8 p.Article
Differences in methylation patterns in the methylation boundary region of IDS gene in hunter syndrome patients: implications for CpG hot spot mutationsTOMATSU, Shunji; SUKEGAWA, Kazuko; COOPER, Alan et al.European journal of human genetics. 2006, Vol 14, Num 7, pp 838-845, issn 1018-4813, 8 p.Article
Advanced renal insufficiency in a 34-year-old man with Lowe syndromeSCHRAMM, Lothar; GAL, Andreas; ZIMMERMANN, Josef et al.American journal of kidney diseases. 2004, Vol 43, Num 3, pp 538-543, issn 0272-6386, 6 p.Article
Disruption of the PDGFB gene in a 1;22 translocation patient does not cause Costello syndromeSUTAJOVA, Markéta; NEUKIRCHEN, Ursula; MEINECKE, Peter et al.Genomics (San Diego, Calif.). 2004, Vol 83, Num 5, pp 883-892, issn 0888-7543, 10 p.Article
Mutations in HPRP3, a third member of pre-mRNA splicing factor genes, implicated in autosomal dominant retinitis pigmentosaCHAKAROVA, Christina F; HIMS, Matthew M; ROSENBERG, Thomas et al.Human molecular genetics (Print). 2002, Vol 11, Num 1, pp 87-92, issn 0964-6906Article
Nonsense Mutations in FAM161A Cause RP28-Associated Recessive Retinitis PigmentosaLANGMANN, Thomas; DI GIOIA, Silvio Alessandro; ARSENIJEVIC, Yvan et al.American journal of human genetics. 2010, Vol 87, Num 3, pp 376-381, issn 0002-9297, 6 p.Article
Phenotypic Variability and Long-term Follow-up of Patients With Known and Novel PRPH2/RDS Gene MutationsRENNER, Agnes B; FIEBIG, Britta S; WEBER, Bernhard H. F et al.American journal of ophthalmology. 2009, Vol 147, Num 3, pp 518-530, issn 0002-9394, 13 p.Article
Trace-based Just-in-Time Type Specialization for Dynamic LanguagesGAL, Andreas; EICH, Brendan; RUDERMAN, Jesse et al.ACM SIGPLAN notices. 2009, Vol 44, Num 6, pp 465-478, issn 1523-2867, 14 p.Conference Paper
Mutations of the mitochondrial holocytochrome c-Type synthase in X-Linked dominant microphthalmia with linear skin defects syndromeWIMPLINGER, Isabella; MORLEO, Manuela; KUTSCHE, Kerstin et al.American journal of human genetics. 2006, Vol 79, Num 5, pp 878-889, issn 0002-9297, 12 p.Article
Novel mutations and repeated findings of mutations in familial Alzheimer diseaseFINCKH, Ulrich; KUSCHEL, Christian; GAL, Andreas et al.Neurogenetics (Oxford. Print). 2005, Vol 6, Num 2, pp 85-89, issn 1364-6745, 5 p.Article