Results of search for 'au:"HARMS, E"' › مکتبة رقمیه للعلوم الطبيه catalog

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- Bauer, H
- Bulla, M
- Denecke, J
- Deufel, T
- Freeze, H H
- Frosch, M
- HARMS, E
- Harms, E
- Harms, E H
- Jorch, G
- Kern, H
- Klöck, F K
- Koch, H G
- Linnebank, M
- Marquardt, T
- Rohde, W
- Rott, R
- Scholtissek, C
- Ullrich, K
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	181.	Intact survival with transfusion-associated graft-versus-host disease proved by human leukocyte antigen typing of lymphocytes in skin biopsy specimens. [electronic resource] by Hentschel, R Broecker, E B Kolde, G Frosch, M Friedrich, W Holzgreve, W Westphal, E Harms, E Producer: 19950209 In: The Journal of pediatrics vol. 126 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	182.	Transcytosis of IgG from the basolateral to the apical membrane of human thyrocytes in autoimmune thyroid disease. [electronic resource] by Zimmer, K P Schmid, K W Böcker, W Scheumann, G F Dralle, H Brämswig, J Harms, E Producer: 19970311 In: Current topics in pathology. Ergebnisse der Pathologie vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	183.	Site-specific mutagenesis of Escherichia coli asparaginase II. None of the three histidine residues is required for catalysis. [electronic resource] by Wehner, A Harms, E Jennings, M P Beacham, I R Derst, C Bast, P Röhm, K H Producer: 19921013 In: European journal of biochemistry vol. 208 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	184.	Colchicine for secondary nephropathic amyloidosis in cystic fibrosis. [electronic resource] by Kuwertz-Bröking, E Koch, H G Schulze Everding, A Bulla, M Dworinczak, B Helmchen, U Harms, E Producer: 19950524 In: Lancet (London, England) vol. 345 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	185.	Expression of S100A12 (EN-RAGE) in cystic fibrosis. [electronic resource] by Foell, D Seeliger, S Vogl, T Koch, H-G Maschek, H Harms, E Sorg, C Roth, J Producer: 20030820 In: Thorax vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	186.	Assessment of tubular reabsorption of sodium, glucose, phosphate and amino acids based on spot urine samples. [electronic resource] by Rossi, R Danzebrink, S Linnenbürger, K Hillebrand, D Grüneberg, M Sablitzky, V Deufel, T Ullrich, K Harms, E Producer: 19950602 In: Acta paediatrica (Oslo, Norway : 1992) vol. 83 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	187.	Individual blood-brain barrier phenylalanine transport determines clinical outcome in phenylketonuria. [electronic resource] by Weglage, J Wiedermann, D Denecke, J Feldmann, R Koch, H G Ullrich, K Harms, E Möller, H E Producer: 20011101 In: Annals of neurology vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	188.	Persistent infection with small colony variant strains of Staphylococcus aureus in patients with cystic fibrosis. [electronic resource] by Kahl, B Herrmann, M Everding, A S Koch, H G Becker, K Harms, E Proctor, R A Peters, G Producer: 19980421 In: The Journal of infectious diseases vol. 177 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	189.	Renal Fanconi syndrome: first sign of partial respiratory chain complex IV deficiency. [electronic resource] by Kuwertz-Bröking, E Koch, H G Marquardt, T Rossi, R Helmchen, U Müller-Höcker, J Harms, E Bulla, M Producer: 20001011 In: Pediatric nephrology (Berlin, Germany) vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	190.	A novel point mutation at codon 269 of the ornithine transcarbamylase (OTC) gene causing neonatal onset of OTC deficiency. [electronic resource] by Zimmer, K P Matsuura, T Colombo, J P Koch, H G Ullrich, K Deufel, T Harms, E Matsuda, I Producer: 19951213 In: Journal of inherited metabolic disease vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	191.	Myeloid-related proteins 8 and 14 are specifically secreted during interaction of phagocytes and activated endothelium and are useful markers for monitoring disease activity in pauciarticular-onset juvenile rheumatoid arthritis. [electronic resource] by Frosch, M Strey, A Vogl, T Wulffraat, N M Kuis, W Sunderkötter, C Harms, E Sorg, C Roth, J Producer: 20000407 In: Arthritis and rheumatism vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	192.	Homocysteine inhibits tumor necrosis factor-induced activation of endothelium via modulation of nuclear factor-kappa b activity. [electronic resource] by Roth, J Goebeler, M Ludwig, S Wagner, L Kilian, K Sorg, C Harms, E Schulze-Osthoff, K Koch, H Producer: 20010920 In: Biochimica et biophysica acta vol. 1540 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	193.	[Spinal muscular atrophy : Time for newborn screening?] [electronic resource] by Vill, K Blaschek, A Schara, U Kölbel, H Hohenfellner, K Harms, E Olgemöller, B Walter, Maggie C Müller-Felber, W Producer: 20190327 In: Der Nervenarzt vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	194.	Unilateral multicystic dysplastic kidney: experience in children. [electronic resource] by Kuwertz-Broeking, E Brinkmann, O A Von Lengerke, H J Sciuk, J Fruend, S Bulla, M Harms, E Hertle, L Producer: 20040419 In: BJU international vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	195.	[Recommendations on the structural prerequisites for perinatal care in Germany]. [electronic resource] by Bauer, K Vetter, K Groneck, P Herting, E Gonser, M Hackelöer, B J Harms, E Rossi, R Hofmann, U Trieschmann, U Producer: 20060518 In: Zeitschrift fur Geburtshilfe und Neonatologie vol. 210 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	196.	Maternal posttraumatic stress response after the birth of a very low-birth-weight infant. [electronic resource] by Kersting, A Dorsch, M Wesselmann, U Lüdorff, K Witthaut, J Ohrmann, P Hörnig-Franz, I Klockenbusch, W Harms, E Arolt, V Producer: 20050322 In: Journal of psychosomatic research vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	197.	Structure of the human argininosuccinate synthetase gene and an improved system for molecular diagnostics in patients with classical and mild citrullinemia. [electronic resource] by Häberle, J Pauli, S Linnebank, M Kleijer, W J Bakker, H D Wanders, R J A Harms, E Koch, H G Producer: 20020621 In: Human genetics vol. 110 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	198.	Fanconi-Bickel syndrome. [electronic resource] by Manz, F Bickel, H Brodehl, J Feist, D Gellissen, K Geschöll-Bauer, B Gilli, G Harms, E Helwig, H Nützenadel, W Producer: 19901227 In: Pediatric nephrology (Berlin, Germany) vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	199.	Fetal hydrops, hyperechogenic arteries and pathological doppler findings at 29 weeks: prenatal presentation of generalized arterial calcification of infancy - a novel mutation in ENPP1. [electronic resource] by Reitter, A Fischer, D Buxmann, H Nitschke, Y Rutsch, F Mottok, A Hansmann, M L Harms, E Louwen, F Schlosser, R Producer: 20091117 In: Fetal diagnosis and therapy vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	200.	Ultrastructural, immunocytochemical and stereological investigation of hepatocytes in a patient with the mutation of the ornithine transcarbamylase gene. [electronic resource] by Zimmer, K P Matsuda, I Matsuura, T Mori, M Colombo, J P Fahimi, H D Koch, H G Ullrich, K Harms, E Producer: 19950921 In: European journal of cell biology vol. 67 Availability: No items available. Save to lists Add to cart (remove)

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