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DIE FEINSTRUKTUR DER KOPF-EPIDERMIS JUNGER REGENBOGENFORELLEN (SALMO GAIRDNERI RICHARDSON). EINE LICHT, TRANSMISSIONS- UND RASTERELEKTRONENMIKROSKOPISCHE UNTERSUCHUNG = L'ULTRASTRUCTURE DE L'EPIDERME DE LA TETE DE LA TRUITE JUVENILE (S.G.R.). ETUDE PAR MICROSCOPIE OPTIQUE, ELECTRONIQUE PAR TRANSMISSION ET PAR BALAYAGEPOHLA GUBO G; POHLA H; ADAM H et al.1981; ZOOL. ANZ.; ISSN 0323-3774; DDR; DA. 1981; VOL. 207; NO 1-2; PP. 1-15; ABS. ENG; BIBL. 3 P.Article

LICHT- UND RASTERELEKTRONENMIKROSKOPISCHE UNTERSUCHUNGEN AN GAUMAN UND ZUNGE DER GELBBAUCHUNKE, BOMBINA VARIEGATA L. = ETUDE PAR MICROSCOPIE OPTIQUE ET ELECTRONIQUE A BALAYAGE DU PALAIS ET DE LA LANGUE DE B.V.L.GUBO G; LAMETSCHWANDTNER A; SIMONSBERGER P et al.1978; ANAT. ANZ.; DDR; DA. 1978; VOL. 144; NO 3; PP. 169-178; ABS. ENG; BIBL. 22 REF.Article

A NEW CELL TYPE IN THE TASTE BUDS OF ANURANS. A SCANNING AND TRANSMISSION ELECTRON MICROSCOPIC STUDY.SAGMEISTER H; GUBO G; LAMETSCHWANDTNER A et al.1977; CELL TISSUE RES.; GERM.; DA. 1977; VOL. 183; NO 4; PP. 553-556; BIBL. 11 REF.Article

Diagnostik bullöser Autoimmun-dermatosen mit subepidermaler Blasenbildung-Untersuchungen an Kochsalz-getrennter Haut (Salt-Split-Methode) = Diagnosis of autoimmune subepidermal bullous diseases. Salt-split skin test = Diagnosis of autoimmune subepidermal bullous disease. Salt-Split skin testPOHLA-GUBO, G; BECHER, E; ROMANI, N et al.H + G. Zeitschrift für Hautkrankheiten. 1993, Vol 68, Num 9, pp 573-580, issn 0301-0481Article

Unilaterale Blepharochalsaiss mit läsionalen IgA-Ablagerungen = Unilateral blepharochalasis with IgA-depositsSCHAEPPI, H; EMBERGER, M; WIELAND, U et al.Hautarzt. 2002, Vol 53, Num 9, pp 613-617, issn 0017-8470Article

'Salt-split' test on normal, non-sun-exposed skin of patients with antoimmune subepidermal bullous diseasesPOHLA-GUBO, G; BECHER, E; ROMANI, N et al.Dermatology (Basel). 1994, Vol 189, issn 1018-8665, p. 123, SUP1Conference Paper

Ocular involvement in IgA-epidermolysis bullosa acquisitaBAUER, J. W; SCHAEPPI, H; METZE, D et al.British journal of dermatology (1951). 1999, Vol 141, Num 5, pp 887-892, issn 0007-0963Conference Paper

Erbliche blasenbildende Erkrankungen : Klinik, Diagnostik und Therapie der Epidermolysis bullosa : Pädiatrische Dermatologie, Teil II = Hereditary blistering diseaes. Symptoms, diagnosis and treatment of epidermolysis bullosaLAIMER, M; LANSCHÜTZER, C. M; NISCHLER, E et al.Der Hautarzt. 2009, Vol 60, Num 5, issn 0017-8470, 378-388 [11 p.]Article

Characteristic immunohistochemical and ultrastructural findings indicate that Kindler's syndrome is an apoptotic skin disorderLANSCHUETZER, C. M; MUSS, W. H; EMBERGER, M et al.Journal of cutaneous pathology. 2003, Vol 30, Num 9, pp 553-560, issn 0303-6987, 8 p.Article

Treatment-resistant classical epidermolysis bullosa acquisita responding to rituximabSADLER, E; SCHAFLEITNER, B; LANSCHUETZER, C et al.British journal of dermatology (1951). 2007, Vol 157, Num 2, pp 417-419, issn 0007-0963, 3 p.Article

A novel homozygous nonsense deletion/insertion mutation in the keratin 14 gene (Y248X; 744delC/insAG) causes recessive epidermolysis bullosa simplex type KöbnerLANSCHUETZER, C. M; KLAUSEGGER, A; POHLA-GUBO, G et al.Clinical and experimental dermatology (Print). 2003, Vol 28, Num 1, pp 77-79, issn 0307-6938, 3 p.Article

Premature termination codons are present on both alleles of the bullous pemphigoid antigen 2/Type XVII collagen gene in five Austrian families with generalized atrophic benign epidermolysis bullosaDARLING, T. N; MCGRATH, J. A; YANCEY, K. B et al.Journal of investigative dermatology. 1997, Vol 108, Num 4, pp 463-468, issn 0022-202XConference Paper

Mapeo por inmunofluorescencia para el diagnóstico de epidermólisis ampollosa congénita = Immunofluorescence Mapping for Diagnosis of Congenital Epidermolysis BullosaCEPEDA-VALDES, R; POHLA-GUBO, G; BORBOLLA-ESCOBOZA, J. R et al.Actas dermo-sifiliográficas (Ed. impresa). 2010, Vol 101, Num 8, pp 673-682, issn 0001-7310, 10 p.Article

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