Zobrazeno 1 - 10
of 178
pro vyhledávání: '"C. Szwarc"'
Publikováno v:
Journal de Pédiatrie et de Puériculture. 17:156-159
Resume Les auteurs rapportent un cas de septicemie dans les suites operatoires immediates d'une appendicite gangrenee. Ils insistent sur le retard diagnostique lie a la diarrhee, signe fonctionnel frequent dans l'appendicite de l'enfant et sur la nec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::97578bc3d8c24980714c77d819eab722
https://doi.org/10.1016/j.jpp.2004.02.001
https://doi.org/10.1016/j.jpp.2004.02.001
Publikováno v:
BJU International. 91:528-531
Objective To describe a surgical method (a modified Duplay technique), and its results, for hypospadias repair, developed to avoid the common complication of fistula. Patients and methods The urethroplasty was modified so that it no longer comprises
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6fa41f728ba10948651b3131281ad45
https://doi.org/10.1046/j.1464-410x.2003.04110.x
https://doi.org/10.1046/j.1464-410x.2003.04110.x
Publikováno v:
La Revue de Médecine Interne. 31:S217-S219
Fabry disease is an X-linked recessive lysosomal storage disorder caused by α-galactosidase A deficiency. Although the disease presents in childhood, diagnosis is often delayed to adulthood or missed, presumably due to the lack of specificity of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0e46987b7c4fffaa1bb9eadf922ec682
https://doi.org/10.1016/s0248-8663(10)70015-1
https://doi.org/10.1016/s0248-8663(10)70015-1
Autor:
Olteanu, Octav1 (AUTHOR)
Publikováno v:
Mathematics (2227-7390). Sep2024, Vol. 12 Issue 18, p2878. 17p.
Autor:
Karabelas, Anastasios J.1 (AUTHOR) alexmoschona@certh.gr, Moschona, Alexandra1 (AUTHOR), Merenidis, Konstantinos1 (AUTHOR)
Publikováno v:
Membranes. Sep2024, Vol. 14 Issue 9, p200. 19p.
Publikováno v:
La Revue de medecine interne. 31
Fabry disease is an X-linked recessive lysosomal storage disorder caused by α-galactosidase A deficiency. Although the disease presents in childhood, diagnosis is often delayed to adulthood or missed, presumably due to the lack of specificity of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7bc6e994fab3f9ed2f2fd066defc6c6b
https://pubmed.ncbi.nlm.nih.gov/21211667
https://pubmed.ncbi.nlm.nih.gov/21211667
Autor:
P, Neville, C, Szwarc, E, Ayadi, H, Lardy, A C, Jimenez, M C, Vaillant, H, Nakajima, D, Sirinelli, A, Chantepie, M, Robert
Publikováno v:
Archives des maladies du coeur et des vaisseaux. 91(9)
Aneurysmal dilatation of a patent ductus arteriosus is a rare condition. One hundred and fifty three cases have been reported, of which 59 (39%) were operated, with an operative mortality of 16%. The authors report a case detected in a premature neon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::dadbc4c258c747cfbf8dcfc5b7e1719a
https://pubmed.ncbi.nlm.nih.gov/9805581
https://pubmed.ncbi.nlm.nih.gov/9805581
Autor:
Olteanu, Cristian Octav1 (AUTHOR) octav.olteanu50@gmail.com
Publikováno v:
Symmetry (20738994). Jun2024, Vol. 16 Issue 6, p757. 14p.
Publikováno v:
Archives de Pédiatrie. 17:141
Entre 1988 et 2008, 64 transplantations du rein ont ete effectuees chez 58 enfants. L’âge moyen etait de 10,8 ans. 22 % des enfants presentaient des vaisseaux multiples. Les complications ont ete etudiees sur 2 periodes successives de 10 ans (n =
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::facec18314a57bf9f8d89132875da6af
https://doi.org/10.1016/s0929-693x(10)70758-2
https://doi.org/10.1016/s0929-693x(10)70758-2
Autor:
A, Maćkowiak, C, Szwarc
Publikováno v:
Klinika oczna. 93(10-11)
In the period of 1972-1973 in the Poznań Department of Ophthalmology were performed 23 operations of scleral infolding with diathermocoagulation in cases of ora serrata dialysis (giant tears were not included in this group). Fifteen years later 20 p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6698c96e2d7fea2c3c8a22a432aabf20
https://pubmed.ncbi.nlm.nih.gov/1821022
https://pubmed.ncbi.nlm.nih.gov/1821022