Výsledky vyhledávání - "T, Torresani"

Geistige Entwicklung bei angeborener Hypothyreose: Ergebnisse einer Umfrage in 14 europäischen Ländern

Autor: R H Largo, Qin Qing, Ruth Illig, M. Klett, P. Rochiccioli, T. Torresani

Publikováno v: DMW - Deutsche Medizinische Wochenschrift. 113:667-671

Although newborn screening for congenital hypothyroidism was introduced into Europe as late as 1975, its high acceptance rate has quickly led to its wide use in most European countries. One would expect early diagnosis with early onset of treatment t

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::b19ac592effebc7c941c076431294960
https://doi.org/10.1055/s-2008-1067701

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ePS01.2 Newborn screening for cystic fibrosis in Switzerland – Evaluation after 5 years

Autor: M. Jurca, C.E. Kuehni, C.S. Rueegg, R. Fingerhut, S. Gallati, T. Torresani, M. Baumgartner, J. Barben

Publikováno v: Journal of Cystic Fibrosis. 15:S36-S37

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ac8ef43d9c454bebb003115e63a68f08
https://doi.org/10.1016/s1569-1993(16)30189-8

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Evolution of an influenza pandemic in 13 countries from 5 continents monitored by protein microarray from neonatal screening bloodspots

Publikováno v: Journal of Clinical Virology, 61(1), 74-80. Elsevier

Background: Because of lack of worldwide standardization of influenza virus surveillance, comparison between countries of impact of a pandemic is challenging. For that, other approaches to allow internationally comparative serosurveys are welcome. Ob

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https://pubmed.ncbi.nlm.nih.gov/25017954

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Urinary Growth Hormone in Growth-Impaired Children with Chronic Inflammatory Bowel Disease

Autor: John Walker-Smith, C. P. Braegger, S H Murch, T T MacDonald, Martin O. Savage, T Torresani

Publikováno v: Journal of Pediatric Gastroenterology and Nutrition. 16:49-52

Growth impairment of undefined aetiology occurs in approximately 30% of children with chronic inflammatory bowel disease. We measured urinary growth hormone concentrations in 36 children with chronic inflammatory bowel disease and 51 normal controls.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6dd0cd40c4bb65d8a179d1067a250899
https://doi.org/10.1097/00005176-199301000-00009

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Contents, Vol. 38, 1992

Autor: Masao Ota, Fausto Zuccato, J. Smitz, P. Rochiccioli, F. Alexandre, T. Torresani, M.T. Tauber, Hideo Sasaki, H. Loeb, H.R. Davies, Massimo Licini, Noriko Ohara, Fernández Martín, R.V.G. García-Mayor, Akira Sekikawa, Ichiro Komiya, Anna Rosa Bussi, Andrade Olivié, Fabio Legati, B. Rogé, Hirofumi Fukushima, P.C. Sizonenko, Johan Auwerx, Ivar K. Rossavik, Maurizio Schettino, Gorm Greisen, I. Dab, G.E. Theintz, J.R. Hawkins, J. De Schepper, E. Flutters, Hiromi Ootsuka, Nobuyuki Takasu, Milo Zachmann, S. Hachimi-Idrissi, M.N. Patterson, C. Páramo, J.-E. Toublanc, S.A. Chalew, D.M. Williams, Afonso Lopes, Takashi Yamada, A. Kowarski, Pankaja S. Venkataraman, Michael R. Waterman, J.C. Galofré, J.A. Batch, Mark A. Brandenburg, William B. Wehrenberg, I.A. Hughes, B.D. Brown, D.J. Hill, B. Sopeña, Diane S. Keeney, B.A.J. Evans, Makoto Tominaga, Z. Zadik, Andrea Giustina

Publikováno v: Hormone Research. 38:I-IV

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::f52033611c3f99a8f69051f465e969bf
https://doi.org/10.1159/000182539

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Serum and follicular fluid insulin like growth factors I and II during growth hormone co-treatment for in-vitro fertilization and embryo transfer

Autor: Christine P. West, E.J. Owen, T. Torresani, Bridgett A. Mason, Howard S. Jacobs

Publikováno v: Clinical Endocrinology. 35:327-334

Summary. objective We wished to assess the changes in serum IGF-I and IGF-ll concentrations during gonadotrophin treatment alone or with additional GH treatment and to compare follicular fluid IGF-I and IGF-II concentrations in the two treatment grou

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https://doi.org/10.1111/j.1365-2265.1991.tb03544.x

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Novel mutations of the thyroid peroxidase gene in patients with permanent congenital hypothyroidism

Autor: C Leitner, Annette Grüters, T Torresani, Petra Ambrugger, Iva Stoeva, Heike Biebermann

Publikováno v: European journal of endocrinology. 145(1)

OBJECTIVE: It is suggested that iodide organification defects account for 10% of all cases with congenital hypothyroidism (CH). One candidate gene for these defects is the thyroid peroxidase (TPO) gene. DESIGN: Exons 2, 8-10 and 14 of the TPO gene we

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2cbf1a2e803d35c82188c4a465d8829b
https://pubmed.ncbi.nlm.nih.gov/11415848

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Evaluation of a clinical algorithm involving serum eosinophil cationic protein for guiding the anti-inflammatory treatment of bronchial asthma in childhood

Autor: A, Prehn, R A, Seger, T, Torresani, L, Molinari, F H, Sennhauser

Publikováno v: Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology. 11(2)

A pilot study was performed to investigate a clinical algorithm using serum-eosinophil cationic protein level (S-ECP) as an objective parameter for tapering the anti-inflammatory treatment in chronic childhood asthma. We studied 21 outpatient asthmat

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::ef8326ecfb5dbd6c78e77d88cb23ab13
https://pubmed.ncbi.nlm.nih.gov/10893010

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The frequency of an inactivating point mutation (566C--T) of the human follicle-stimulating hormone receptor gene in four populations using allele-specific hybridization and time-resolved fluorometry

Autor: M, Jiang, K, Aittomäki, C, Nilsson, P, Pakarinen, A, Iitiä, T, Torresani, H, Simonsen, V, Goh, K, Pettersson, A, de la Chapelle, I, Huhtaniemi

Publikováno v: The Journal of clinical endocrinology and metabolism. 83(12)

We have described previously in the Finnish population an inactivating point mutation (566C--T) in the human FSH receptor (FSHR) gene. In women, this mutation causes hypergonadotropic ovarian failure with arrest of follicular maturation and infertili

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::0c30db344e4af5c89610cbeef2400809
https://pubmed.ncbi.nlm.nih.gov/9851774

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[Transitory neonatal hypothyroidism caused by transplacental transfer of anti-receptor antibodies of hypophyseal thyroid simulation. Case report and estimated incidence]

Autor: S, Pasquier, T, Torresani, E, Werder, H E, Gnehm

Publikováno v: Schweizerische medizinische Wochenschrift. 127(44)

Transient neonatal hypothyroidism induced by transplacental transfer of thyrotropin receptor-blocking antibodies is rare, but should be diagnosed early because its course, treatment, and prognosis are different from the other forms of congenital hypo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::a1d9a294063b4a2efa8fd8e9779d2879
https://pubmed.ncbi.nlm.nih.gov/9446201

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