Beyond art and beauty in search of the object of philosophical aesthetics = Au-delà de l'art et de la beauté: la quête de l'objet de l'esthétique philosophiqueSPEER, A.International journal of philosophical studies. 2000, Vol 8, Num 1, pp 73-88, issn 0967-2559Article

Wissenschaft und Erkenntnis : Zur Wissenschaftslehre BonaventurasSPEER, A.Wissenschaft und Weisheit. 1986, Vol 49, Num 2-3, pp 168-198, issn 0043-678XArticle

Mensch und Natur im Mittelalter. Tagungsberich von der 27. Kölner MediaevistentagungSPEER, A.Bulletin de Philosophie Médiévale. 1990, Num 32, pp 222-226Article

ISOLATION AND CHARACTERIZATION OF HUMAN LIVER MRNA = ISOLEMENT ET CARACTERISATION D'ARNM DE FOIE HUMAINSPEER A; THIELE B; LIEBSCHER DH et al.1981; ACTA BIOL. MED. GER.; ISSN 0001-5318; DDR; DA. 1981; VOL. 40; NO 9; PP. 1095-1100; ABS. GER; BIBL. 23 REF.Article

Fine mapping of human PI 3-kinase associated p85α transcripts in the YAC contig surrounding the spinal muscular atrophy geneHUSCHENBETT, J; GASCH, A; KATZER, A et al.Human genetics. 1994, Vol 94, Num 4, pp 427-431, issn 0340-6717Article

Polymorphism in the human E-selectin gene detected by PCR-SSCPWENZEL, K; HANKE, R; SPEER, A et al.Human genetics. 1994, Vol 94, Num 4, pp 452-453, issn 0340-6717Article

Point mutations at the carboxy terminus of the human dystrophin gene: implications for an association with mental retardation in DMD patientsLENK, U; HANKE, R; THIELE, H et al.Human molecular genetics (Print). 1993, Vol 2, Num 11, pp 1877-1881, issn 0964-6906Article

Prenatal diagnosis of the acute form of proximal spinal muscular atrophy : experience on the acceptance of linkage analyses by the familiesHUSCHENBETT, J; HANKE, R; PFEIFER, L et al.Prenatal diagnosis. 1993, Vol 13, Num 7, pp 643-649, issn 0197-3851Article

The relationship between preceptor expectations and student performance on 2 pediatric objective structured clinical examination stationsMALLOY, M. H; PERKOWSKI, L; CALLAWAY, M et al.Archives of pediatrics & adolescent medicine. 1998, Vol 152, Num 8, pp 806-811, issn 1072-4710Article

Four new polymorphisms in the human dystrophin gene from an Argentinian populationBARANZINI, S. E; LENK, U; SZIJAN, I et al.Muscle & nerve. 1997, Vol 20, Num 11, pp 1451-1453, issn 0148-639XArticle

Alternative splicing of dystrophin mRNA complicates carrier determination : report of a DMD familyLENK, U; DEMUTH, S; KRÄFT, U et al.Journal of medical genetics. 1993, Vol 30, Num 3, pp 206-209, issn 0022-2593Article

Biliary ascariasis : a worm in the ductKOLT, S. D; WIRTH, P. D; SPEER, A. G et al.Medical journal of Australia. 1991, Vol 154, Num 9, pp 629-630, issn 0025-729XArticle

Mapping of a human rRNA gene in the YAC contig surrounding the SMA candidate geneHUSCHENBETT, J; GASCH, A; KATZER, A et al.Human genetics. 1995, Vol 96, Num 3, pp 335-338, issn 0340-6717Article

Introduction of genomic diagnosis of classical phenylketonuria to the health care system of the German Democratic RepublicRIESS, O; MICHEL, A; SPEER, A et al.Clinical genetics. 1987, Vol 32, Num 4, pp 209-215, issn 0009-9163Article

The altruistic personality : in what contexts is is apparent ?CARLO, G; EISENBERG, N; TROYER, D et al.Journal of personality and social psychology. 1991, Vol 61, Num 3, pp 450-458, issn 0022-3514Article

Development of a DNA-adsorbent for the specific removal of anti-DNA autoantibodies in systemic lupus erythematousus (SLE)HIEPE, F; WOLBART, K; SCHOSSLER, W et al.Biomaterials, artificial cells and artificial organs. 1990, Vol 18, Num 5, pp 683-688, issn 0890-5533, 6 p.Article

Use of cyanuric chloride-activated paper for detection of subpicogram quantities of specific DNA sequences and its application to linked restriction fragment length polymorphism analysis in a Duchenne muscular dystrophy affected familyHUNGER, H.-D; SPEER, A; FLACHMEIER, C et al.Analytical biochemistry. 1987, Vol 165, Num 1, pp 45-55, issn 0003-2697Article

Genomic organization of the human excitatory amino acid transporter gene GLT-1MEYER, T; LUDOLPH, A. C; MORKEL, M et al.Neuroreport (Oxford). 1997, Vol 8, Num 3, pp 775-777, issn 0959-4965Article

Studies of the coding region of the neuronal glutamate transporter gene in amyotrophic lateral sclerosisMEYER, T; LENK, U; KÜTHER, G et al.Annals of neurology. 1995, Vol 37, Num 6, pp 817-819, issn 0364-5134Article

Non-isotopic analysis of single strand conformation polymorphism (SSCP) in the exon 13 region of the human dystrophin geneLENK, U; HANKE, R; KRÄFT, U et al.Journal of medical genetics. 1993, Vol 30, Num 11, pp 951-954, issn 0022-2593Article

Linkage disequilibrium between RFLP haplotype 2 and the affected PAH allele in PKU families from the Berlin area of the German Democratic RepublicRIESS, O; MICHEL, A; SPEER, A et al.Human genetics. 1988, Vol 78, Num 4, pp 343-346, issn 0340-6717Article

Creating and evaluating an independent ambulatory internal medicine clerkshipROSEBRAUGH, C. J; SZAUTER, K; AINSWORTH, M. A et al.The American journal of the medical sciences. 1998, Vol 315, Num 1, pp 30-34, issn 0002-9629Article

Molecular analysis of Duchenne and Becker muscular dystrophiesLOVE, D. R; FORREST, S. M; SMITH, T. J et al.British medical bulletin. 1989, Vol 45, Num 3, pp 659-680, issn 0007-1420Article

A cysteine 3340 substitution in the dystroglycan-binding domain of dystrophin associated with Duchenne muscular dystrophy, mental retardation and absence of the ERG b-waveLENK, U; OEXLE, K; VOIT, T et al.Human molecular genetics (Print). 1996, Vol 5, Num 7, pp 973-976, issn 0964-6906, 3 p.Article

RFLP-discordance within the human phenylalanine hydroxylase locusRIESS, O; MICHEL, A; BERGER, W et al.Human genetics. 1989, Vol 83, Num 2, pp 199-201, issn 0340-6717Article