MAST CELLS IN CLUSTER HEADACHECUYPERS J; WESTPHAL K; BUNGE S et al.1980; ACTA NEUROL. SCAND.; DNK; DA. 1980; VOL. 61; NO 5; PP. 327-329; BIBL. 9 REF.Article

THERAPY OF CLUSTER HEADACHE WITH HISTAMINE H₁ AND H₂ RECEPTOR ANTAGONISTSCUYPERS J; ALTENKIRCH H; BUNGE S et al.1979; EUROP. NEUROL.; CHE; DA. 1979; VOL. 18; NO 5; PP. 345-347; BIBL. 10 REF.Article

BEDEUTUNG VON PRAEDISPONIERENDEN FAKTOREN UND PERSOENLICHKEITSZUEGEN BEI CLUSTER-KOPFSCHMERZ-PATIENTEN = INFLUENCE DES FACTEURS PREDISPOSANTS ET DE LA PERSONNALITE SUR LA MALADIE DE HORTONCUYPERS J; ALTENKIRCH H; BUNGE S et al.1980; FORTSCHR. NEUROL. PSYCHIATR. IHRER GRENZGEB.; ISSN 0015-8194; DEU; DA. 1980; VOL. 48; NO 12; PP. 643-647; ABS. ENG; BIBL. 16 REF.Article

PERSONALITY PROFILES IN CLUSTER HEADACHE AND MIGRAINECUYPERS J; ALTENKIRCH H; BUNGE S et al.1981; HEADACHE; ISSN 0017-8748; USA; DA. 1981; VOL. 21; NO 1; PP. 21-24; BIBL. 13 REF.Article

Nachträgliche universelle Einkapselung von Altlasten = Environmental dangerous situations resulting from contamined sites can be reduced or even eliminated for langer time by incapsulationsBAYER, H.-J; CALDONAZZI, O; BUNGE, S et al.Energieanwendung und Energietechnik. 1994, Vol 43, Num 8, pp 317-320, issn 0944-3169Article

A comparison of leaf thionin sequences of barley cultivars and wild barley cultivars and wild barley speciesBUNGE, S; WOLTERS, J; APEL, K et al.MGG. Molecular & general genetics. 1992, Vol 231, Num 3, pp 460-468, issn 0026-8925Article

Reversal of relative thresholds for synaptic facilitation and increased excitability induced by serotonin and tail nerve stimulation in Aplysia sensory neuronsBUNGE, S. A; MAUELSHAGEN, J; CAREW, T. J et al.Neurobiology of learning and memory (Print). 1997, Vol 67, Num 3, pp 259-263, issn 1074-7427Article

Plasma glucose and free fatty acids modulate the secretion of growth hormoçne, but not prolactin, in the rhesus and java monkeyQUABBE, H.-J; BUNGE, S; WALZ, T et al.The Journal of clinical endocrinology and metabolism. 1990, Vol 70, Num 4, pp 908-915, issn 0021-972X, 8 p.Conference Paper

Evidence for an iduronate-sulfatase pseudogene near the functional Hunter syndrome gene in Xq27.3-q28RATHMANN, M; BUNGE, S; STEGLICH, C et al.Human genetics. 1995, Vol 95, Num 1, pp 34-38, issn 0340-6717Article

Neural correlates of tic severity and cognitive control in children with Tourette syndromeBAYM, C. L; CORBETT, B. A; WRIGHT, S. B et al.Brain. 2008, Vol 131, pp 165-179, issn 0006-8950, 15 p., 1Article

Examining cortisol rhythmicity and responsivity to stress in children with Tourette syndromeCORBETT, B. A; MENDOZA, S. P; BAYM, C. L et al.Psychoneuroendocrinology. 2008, Vol 33, Num 6, pp 810-820, issn 0306-4530, 11 p.Article

Common CFTR mutations are not likely to predispose to chronic bronchitis in Northern GermanyARTLICH, A; BOYSEN, A; BUNGE, S et al.Human genetics. 1995, Vol 95, Num 2, pp 226-228, issn 0340-6717Article

Mucopolysaccharidosis type II (Hunter syndrome) : Mutation hot spots in the iduronate-2-sulfatase geneRATHMANN, M; BUNGE, S; BECK, M et al.American journal of human genetics. 1996, Vol 59, Num 6, pp 1202-1209, issn 0002-9297Article

Iduronate-2-sulfatase gene mutations in 16 patients with mucopolysaccharidosis type II (Hunter syndrome)BUNGE, S; STEGLICH, C; ZUTHER, C et al.Human molecular genetics (Print). 1993, Vol 2, Num 11, pp 1871-1875, issn 0964-6906Article

Mucopolysaccharidosis type IIIB (Sanfilippo B) : identification of 18 novel α-N-acetylglucosaminidase gene mutationsBUNGE, S; KNIGGE, A; STEGLICH, C et al.Journal of medical genetics. 1999, Vol 36, Num 1, pp 28-31, issn 0022-2593Article

Mutation analysis of the iduronate-2-sulfatase gene in patients with mucopolysaccharidosis type II (Hunter syndrome)BUNGE, S; STEGLICH, C; BECK, M et al.Human molecular genetics (Print). 1992, Vol 1, Num 5, pp 335-339, issn 0964-6906Article

Novel mutations in Sanfilippo A syndrome : implications for enzyme functionWEBER, B; GUO, X.-H; WRAITH, J. E et al.Human molecular genetics (Print). 1997, Vol 6, Num 9, pp 1573-1579, issn 0964-6906Article

Prenatal diagnosis and carrier detection in mucopolysaccharidosis type II mutation analysis. A 47,XXY male hterozygous for a missense point mutationBUNGE, S; STEGLICH, C; LORENZ, P et al.Prenatal diagnosis. 1994, Vol 14, Num 9, pp 777-780, issn 0197-3851Article

Molecular analysis in patients with mucopolysaccharidosis type II suggests that DXS466 maps within the Hunter geneSTEGLICH, C; BUNGE, S; HULSEBOS, T et al.Human genetics. 1993, Vol 92, Num 2, pp 179-182, issn 0340-6717Article

Anderson-Fabry disease: Clinical manifestations of disease in female heterozygotesWHYBRA, C; KAMPMANN, Chr; WILLERS, I et al.Journal of inherited metabolic disease. 2001, Vol 24, Num 7, pp 715-724, issn 0141-8955Article

Molecular analysis and genetic mapping of the rhodopsin gene in families with autosomal dominant retinitis pigmentosaBUNGE, S; WEDEMANN, H; SCHINZEL, A et al.Genomics (San Diego, Calif.). 1993, Vol 17, Num 1, pp 230-233, issn 0888-7543Article

Prefrontal and hippocampal contributions to visual associative recognition: Interactions between cognitive control and episodic retrievalBUNGE, S. A; BURROWS, B; WAGNER, A. D et al.Brain and cognition (Print). 2004, Vol 56, Num 2, pp 141-152, issn 0278-2626, 12 p.Article

Clinical, biochemical and molecular findings in a two-generation Morquio A familyTYLKI-SZYMANSKA, A; CZARTORYSKA, B; BUNGE, S et al.Clinical genetics. 1998, Vol 53, Num 5, pp 369-374, issn 0009-9163Article

Mucopolysaccharidosis type I: identification of 8 novel mutations and determination of the frequency of the two common α-L-iduronidase mutations (W402X) and (Q70X) among European patientsBUNGE, S; KLEIJER, W. J; STEGLICH, C et al.Human molecular genetics (Print). 1994, Vol 3, Num 6, pp 861-866, issn 0964-6906Article

Low-valent metals as reductive cross-linking agents : A new strategy for smoke suppression of poly(vinyl chloride)PIKE, R. D; STARNES, W. H; MACKO, J. A et al.Macromolecules. 1997, Vol 30, Num 22, pp 6957-6965, issn 0024-9297Article