Zobrazeno 1 - 10
of 415
pro vyhledávání: '"I, Daire"'
Autor:
Torun, Arzu
Bu çalışmada Manisa İl Halk Kütüphanesi Yazma Eserler Bölümünde ?45 Hk 1479? numarada kayıtlı olan Muvakkıt Mustafa Bin Rumi tarafından 16. yüzyılda yazılmış Hall-i Daire-i Muaddil incelenmiştir. Hall; karışık bir işi sona erdi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_____10208::c2b8addafeb42d2e0fc9ac5972b11744
https://acikbilim.yok.gov.tr/handle/20.500.12812/600032
https://acikbilim.yok.gov.tr/handle/20.500.12812/600032
Publikováno v:
Archives de Pédiatrie. 13:588-591
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d4518ed6633b0ccf9f7504ae110ecc59
https://doi.org/10.1016/j.arcped.2006.03.060
https://doi.org/10.1016/j.arcped.2006.03.060
Publikováno v:
Archives de Pédiatrie. 13:269-272
We report a case of macroamylasemia in an 11-year-old boy. We compare our clinical and paraclinical data with those described in pediatric literature. Macroamylase resulted in a complex of amylase and immuglobulin. Its fortuitous detection did not re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::711745b9539b972e77f62fb8323f282f
https://doi.org/10.1016/j.arcped.2004.12.022
https://doi.org/10.1016/j.arcped.2004.12.022
Autor:
YEŞİL, GÖZDE, Lebre, Anne Sophie, Dos Santos, Sofia, Guran, Omer, Ozahi, Ilke Ipek, Daire, Valeria Cormier, GÜRAN, TÜLAY
Stuve-Wiedemann Syndrome (SWS) (OMIM #601559) is an autosomal recessive disorder characterized by skeletal changes, bowing of the lower limb, severe osteoporosis and joint contractures, episodic hyperthermia, frequent respiratory infections, feeding
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______9651::8a812c9c8672da453a3724c6f02dec5f
https://hdl.handle.net/20.500.12645/10354
https://hdl.handle.net/20.500.12645/10354
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 13(6)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3e0d1010f8aa26085e0770cfa3e22384
https://pubmed.ncbi.nlm.nih.gov/16697566
https://pubmed.ncbi.nlm.nih.gov/16697566
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 13(3)
We report a case of macroamylasemia in an 11-year-old boy. We compare our clinical and paraclinical data with those described in pediatric literature. Macroamylase resulted in a complex of amylase and immuglobulin. Its fortuitous detection did not re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c6a2c5a28d5904893129eedffba35d47
https://pubmed.ncbi.nlm.nih.gov/16434172
https://pubmed.ncbi.nlm.nih.gov/16434172
Publikováno v:
Archives de Pédiatrie. 15:949
Nous rapportons un cas de pancreatite chronique chez une fillette de 12 ans presentant une mutation des genes PRSS1 (pR116C) et SPINK1 (pN34S). Observation A l’âge de 10 ans, une fille sans antecedents particuliers ni familiaux est hospitalisee po
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0a1354c57a2211a13ada542cdd393c7e
https://doi.org/10.1016/s0929-693x(08)72150-x
https://doi.org/10.1016/s0929-693x(08)72150-x
Autor:
Eden, Alp1, Takıcak, S. Betül2 sbtakicak@kastamonu.edu.tr
Publikováno v:
Studies in Ottoman Science / Osmanlı Bilimi Araştırmaları. 2024, Vol. 25 Issue 1, p1-28. 28p.
Autor:
ERTÜRKMEN, Duygu1 derturkmen@mersin.edu.tr, NOORI, Ahmad Reshad2
Publikováno v:
Gümüshane Üniversitesi Fen Bilimleri Enstitüsü Dergisi. 2023, Vol. 13 Issue 4, p1019-1032. 14p.
Autor:
TORAMAN, Ömer1 omertoraman25@gmail.com
Publikováno v:
Firat University Journal of Social Sciences / Firat Üniversitesi Sosyal Bilimler Dergisi. Sep2023, Vol. 33 Issue 3, p1453-1470. 18p.