Výsledky vyhledávání - "Ulrich V. Willi"

Outcome after prenatal diagnosis of congenital anomalies of the kidney and urinary tract

Autor: Giuseppina Spartà, Josef Wisser, Rita Gobet, Ulrich V. Willi, Guido F. Laube, Thomas J. Neuhaus, Samuel Nef, Marcus Weitz, Kathrin Buder

Congenital anomalies of the kidney and urinary tract are common findings on fetal ultrasound. The aim of this prospective observational study was to describe outcome and risk factors in 115 patients born 1995-2001. All prenatally diagnosed children w

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b33f5ff4b121d227aa58a0c194cabc8a

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Randomised trial of oral versus sequential intravenous/oral cephalosporins in children with pyelonephritis

Autor: Luciano Molinari, Sergio Stocker, Gian Bischoff, Thomas J. Neuhaus, Philippe Goetschel, Christoph Rudin, Daniela B. Husarik, Katja Buechner, U. Hunziker, Ulrich V. Willi, Eric Girardin, Paloma Maria Parvex, Christoph Berger, David Nadal, Alain Gervaix

Publikováno v: European journal of pediatrics, Vol. 167, No 9 (2008) pp. 1037-47

The hypothesis was tested that oral antibiotic treatment in children with acute pyelonephritis and scintigraphy-documented lesions is equally as efficacious as sequential intravenous/oral therapy with respect to the incidence of renal scarring. A ran

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a0974f0aef56495acf7a2398511593c
https://doi.org/10.1007/s00431-007-0638-1

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Hepatic steatosis: a frequent non-specific finding in HIV-infected children

Autor: Thomas Stallmach, Christian Braegger, Ulrich V. Willi, Manuela Albisetti, David Nadal

Publikováno v: European Journal of Pediatrics. 158:971-974

Thirty HIV-infected children were cross-sectionally examined for morphologic hepatic abnormalities, using ultrasonography or histology. Abdominal ultrasonography was performed in 27 children. The liver structure was normal in four patients, one of wh

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4556cdd7996ddfed0a7467adedad73c
https://doi.org/10.1007/s004310051260

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Successful Treatment of Invasive Aspergillosis in Chronic Granulomatous Disease by Bone Marrow Transplantation, Granulocyte Colony-Stimulating Factor–Mobilized Granulocytes, and Liposomal Amphotericin-B

Autor: Hans C. Steinert, Reinhard Seger, Irene Müller, Ulrich V. Willi, Roger Lauener, Mahmut Ozsahin, Hulya Ozsahin, P. Tuchschmid, Maya von Planta, Nigel E.A. Crompton, David Nadal

Publikováno v: Blood. 92:2719-2724

X-linked chronic granulomatous disease (X-CGD) is a primary immunodeficiency with complete absence or malfunction of the nicotinamide adenine dinucleotide phosphate (NADPH) oxidase in the phagocytic cells. Life-threatening infections especially with

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::4d2bba02077506451e300d383d6b0d90
https://doi.org/10.1182/blood.v92.8.2719

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Meningeal hemangiopericytoma in childhood

Autor: Ulrich V. Willi, Ernst Martin, G. M. Kacl, Sebastian Brandner, Felix Niggli, Thierry A.G.M. Huisman

Publikováno v: European Radiology. 10:1073-1075

Meningeal hemangiopericytoma (MHP) is extremely rare in childhood. Mean age at diagnosis is between 38 and 43 years. We present an 8-year-old boy with MHP of the middle cranial fossa. Imaging findings were indistinguishable from an aggressive bone tu

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https://doi.org/10.1007/s003309900222

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MRI and CT of a haemangioma of the mandible in Kasabach-Merritt syndrome

Autor: C. Berger, E. Martin, A. Valavanis, C. Panow, Ulrich V. Willi

Publikováno v: Neuroradiology. 42:215-217

Since the description in 1940 of Kasabach-Merritt syndrome (KMS) in patients with capillary haemangiomas, several other vascular tumours have been recognised as possible causes of this coagulopathy. The literature suggests a specific histological pat

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70c2edd97631d037b1ab34e9d6207e39
https://doi.org/10.1007/s002340050050

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Testicular adrenal-like tissue (TALT) in congenital adrenal hyperplasia: Detection by ultrasonography

Autor: M Atares, Ulrich V. Willi, A. Prader, M Zachmann

Publikováno v: Pediatric Radiology. 21:284-287

In a consecutive series of 15 male adolescents and young adults with congenital adrenal hyperplasia (CAH), the size, shape, firmness and echostructure of the testes were assessed. The latter was abnormal in 7 patients under long standing treatment wi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4096d419305ee43782b22ed530b653c0
https://doi.org/10.1007/bf02018626

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Unknown syndrome: ischiadic hypoplasia, renal dysfunction, immunodeficiency, and a pattern of minor congenital anomalies

Autor: Ulrich V. Willi, A Giedion, Albert Schinzel, R Seger, A Bottani, Christian Braegger, E Leumann, F Hallé

Publikováno v: Journal of Medical Genetics. 28:56-59

We report a 6 year old male with a pattern of malformations and anomalies including intrauterine growth retardation, microcephaly, psychomotor retardation, a pattern of craniofacial anomalies (flat face, hypertelorism, epicanthic folds, strabismus, s

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81d357532a4316d44a7a02622748879a
https://doi.org/10.1136/jmg.28.1.56

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