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Publikováno v:
Journal of Pediatric Critical Care, Vol 5, Iss 3, Pp 94-97 (2018)
Factor X deficiency is one of the rare inherited coagulation disorders. Symptoms vary from mild to severe with the commonest being epistaxis, gum bleeds and menorrhagia. The diagnosis is suspected when both PT and aPTT are prolonged and remains uncor
Externí odkaz:
https://doaj.org/article/31a4c41290d3477198571167ddb51317
Publikováno v:
Journal of Pediatric Critical Care, Vol 5, Iss 3, Pp 94-97 (2018)
Factor X deficiency is one of the rare inherited coagulation disorders. Symptoms vary from mild to severe with the commonest being epistaxis, gum bleeds and menorrhagia. The diagnosis is suspected when both PT and aPTT are prolonged and remains uncor
Publikováno v:
The Indian Journal of Pediatrics. 60:451-454
Adults accompanying 64 children attending a hospital out-patient clinic were questioned about treatment and injections given for illnesses in the previous month. Half the children had received injections, almost all given by private doctors: we consi
Conference
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Akademický článek
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Autor:
Shah VM; Aravind Eye Hospital & Postgraduate Institute of Ophthalmology, Coimbatore, India., Ranjan R; Aravind Eye Hospital & Postgraduate Institute of Ophthalmology, Coimbatore, India., Jeste M; Aravind Eye Hospital & Postgraduate Institute of Ophthalmology, Coimbatore, India., MacIntosh P; Ophthalmic Plastic & Reconstructive Surgery and Neuro-Ophthalmology, Illinois Eye and Ear Infirmary, Chicago, USA., Ashwath D; Department of Pediatrics, Kovai Medical Centre and Hospital, Coimbatore, India.
Publikováno v:
GMS ophthalmology cases [GMS Ophthalmol Cases] 2020 Jun 29; Vol. 10, pp. Doc28. Date of Electronic Publication: 2020 Jun 29 (Print Publication: 2020).