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137 results on '"Schindera F"'

2. Large-scale targeted sequencing comparison highlights extreme genetic heterogeneity in nephronophthisis-related ciliopathies

Author

Schueler, Markus, Halbritter, Jan, Phelps, Ian G, Braun, Daniela A, Otto, Edgar A, Porath, Jonathan D, Gee, Heon Yung, Shendure, Jay, OʼRoak, Brian J, Lawson, Jennifer A, Nabhan, Marwa M, Soliman, Neveen A, Doherty, Dan, Hildebrandt, Friedhelm, Yalcinkaya, F, Bakkaloglu, S, Ozaltin, F, Comak, E, Krull, F, Schmitz-Hübner, Rupprecht, H, Muller, D, Dahlem, P, Hoppe, B, Wolfe, M, Weber, M, Vester, U, Bonzel, K, Nikolay, J, Hansmann, I, Wiefel, M, Orth, U, Pfleiderer, H, Pape, L, Morlot, Ehrich, J, Tonshoff, B, Schindera, F, Hoefele, J, Griebel, M, Broeking, E, Konrad, M, Radke, M, Brandis, M, Kirchhoff, A, Feygina, V, Springate, J, Ahmadzdeh, S, Gipson, D, Becker, A, Dharnidharka, V, Mark, P, Srivaths, P, Wilson, A, Kamil, E, Why, S, Pan, C, Kashtan, C, D’Alessandri, C, Trachtman, H, Kaplan, B, Joseph, M, Weiss, R, Thomas, S, Newberry, L, Koyun, M, Fathy, H, RybiSzuminska, A, Szczepanska, M, Dolezel, Z, Malina, M, Seeman, T, Honzik, T, Ferreira, P, Ferguson, M, Harvey, E, Chong, K, Sandford, R, Josifova, D, Bockenhauer, D, Sayer, J, Johnson, C, Senguttuvan, P, Pela, I, Knops, N, Levart, T, Neuhaus, T, Ayuso, C, Kindi, A, Knoers, N, Antignac, C, Radauer, W, Genzani, C, Berg, U, Klingenberg, C, Jones, C, Savarirayan, R, and Kausman, J

Published
2016
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7. Congenital Cystic Adenomatoid Malformation of the Lung

Author

Becker, M. R., Schindera, F., Maier, W. A., Bill, A. H., editor, Boix-Ochoa, J., editor, Ferguson, C. C., editor, Ghandi, R. K., editor, Gans, S. L., editor, Haller, J. A., editor, Kasai, M., editor, Knutrud, O., editor, Lister, J., editor, Myers, N. A., editor, and Wurnig, Peter, editor

Published
1987
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12. Miscellaneous

Author

Behrenbeck, D. W., Dörge, A., Reinhardt, H. W., Gekle, D., Rostock, D., Kurth, G., Renschler, H. E., Jaenkner, D., Kammerer, E., Thoma, R., Mertz, D. P., Schindera, F., Grossmann, D. F., Frey, J., Peters, Georges, editor, and Roch-Ramel, Françoise, editor

Published
1969
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14. Sonographisch geführte Vorbereitung zur Dünndarmbiopsie mit der Watson-Kapsel - signifikant verringerte Strahlenbelastung

Author

Rösiger A, Prömpeler-Kuhn K, Seitz B, and Schindera F

Subjects
medicine.medical_specialty, medicine.diagnostic_test, Diagnostic ultrasound, business.industry, digestive, oral, and skin physiology, Pylorus, digestive system, digestive system diseases, Small intestine, Catheter, medicine.anatomical_structure, Biopsy, medicine, Watson capsule, Radiology, Nuclear Medicine and imaging, Radiology, business
Abstract

Diagnostic ultrasound showed that the passing of the Watson capsule through the pylorus can be proved demonstrating its catheter within the pylorus. Only the biopsy itself has to be done under radiologic control which results in decreasing X-ray time from sometimes six minutes to a few seconds, usually less than one minute.

Published
2008

37. Purpura Schoenlein-Henoch

Author

Niederhoff, H., primary, Pernice, W., additional, Sedlacek, H., additional, Schindera, F., additional, Schütte, B., additional, and Straßburg, H.-M., additional

Published
1979
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43. Zur Therapie des hämolytisch-urämischen Syndroms

Author

Schindera F, H. Wehinger, Wilhelm Künzer, and Sutor Ha

Subjects
medicine.medical_specialty, Aspirin, business.industry, medicine.medical_treatment, Streptokinase, General Medicine, Heparin, Gastroenterology, Peritoneal dialysis, Dipyridamole, Internal medicine, Platelet adhesiveness, medicine, business, medicine.drug
Published
1974

44. Platelets in the Urine: Further Evidence

Author

Ketelsen Up, Sutor Ah, and Schindera F

Subjects
medicine.medical_specialty, Endocrinology, Chemistry, Internal medicine, medicine, Platelet, Hematology, Urine
Published
1976

47. [Life threatening salicylate poisoning caused by percutaneous absorption in severe ichthyosis vulgaris].

Author

Germann R, Schindera I, Kuch M, Seitz U, Altmeyer S, and Schindera F

Subjects
Acid-Base Equilibrium drug effects, Acid-Base Equilibrium physiology, Administration, Topical, Child, Critical Care, Dose-Response Relationship, Drug, Drug Overdose blood, Drug Overdose therapy, Humans, Ichthyosis Vulgaris blood, Keratolytic Agents administration & dosage, Keratolytic Agents pharmacokinetics, Male, Renal Dialysis, Salicylates administration & dosage, Salicylates pharmacokinetics, Salicylic Acid, Drug Overdose diagnosis, Ichthyosis Vulgaris drug therapy, Keratolytic Agents poisoning, Salicylates poisoning, Skin Absorption physiology
Abstract

In a 7-year-old boy, ichthyosis vulgaris was treated with a 10% ointment for application over a large area of the body surface. In this way, the child received 400 g salicylic acid (0.6 g/kg body weight per day) percutaneously over a period of 4 weeks. The patient was referred to hospital by the family doctor: he was in a deep somnolent state, apparently caused by hyperventilation following wheezing, vomiting, tinnitus and vertigo. Salicylate intoxication was suspected because of metabolic acidosis, an anion gap and respiratory overcompensation. The diagnosis was confirmed by a serum salicylate level of 985 micrograms/ml (therapeutic level 150-300 micrograms/ml). Following forced diuresis and alkalization with sodium bicarbonate, haemodialysis was unnecessary. As the salicylate level declined to values within the therapeutic range, the patient started to recover consciousness, waking on the 4th day. By day 6 there were still obvious neurological deficiencies. Fecal incontinence, bilateral ptosis and intermittent diverging strabismus on the right persisted for some weeks. It was 6 months before complete neurological resolution was achieved. The pathogenesis of salicylate toxicity and the need for safer therapies for ichthyosis vulgaris are discussed.

Published
1996
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49. [Bacterial meningitis after the neonatal period].

Author

Schindera F

Subjects
Age Factors, Child, Preschool, Humans, Infant, Prognosis, Meningitis, Bacterial diagnosis, Meningitis, Bacterial etiology, Meningitis, Bacterial therapy
Published
1995

50. [Clinical features, pathogenesis, and therapy of hereditary angioneurotic edema (author's transl)].

Author

Schindera F, Struck E, and Spira W

Subjects
Adolescent, Adult, Androgens therapeutic use, Angioedema diagnosis, Angioedema drug therapy, Complement C1s deficiency, Female, Humans, Male, Pregnancy, Prognosis, Angioedema genetics
Abstract

The hereditary angioneurotic edema is probably a more frequent disease than presumed until now. It is inherited as an autosomal dominant trait, and is due to diminished or functionally deficient C1 esterase inhibitor. Family history is negative in cases of spontaneous mutations. Two thirds of the patients are already affected in infancy with peripheral edema, facial edema, abdominal symptoms and/or edema of the glottis occuring spontaneously or secondary to trauma. Recently the prognosis has become better due to early diagnosis and the possibility of substitution therapy with C1 esterase inhibitor. A long-term prophylaxis may be achieved with synthetic androgens.

Published
1982

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