يعرض 1 - 4 نتائج من 4 نتيجة بحث عن '"Astha Sarda"', وقت الاستعلام: 1.00s تنقيح النتائج
  1. 1
    دورية أكاديمية
    Masson’s Haemangioma Presenting as a Fibrolipoma

    المؤلفون: Astha Sarda, Murugappan Nachiappan

    المصدر: Journal of Clinical and Diagnostic Research, Vol 10, Iss 5, Pp PD07-PD08 (2016)

    مصطلحات موضوعية: angiosarcoma, masson’s tumour, haemangioendotheliome vegetant intravasculaire, Medicine

    وصف الملف: electronic resource

    Relation: https://jcdr.net/articles/PDF/7808/19670_CE(RA1)_F(T)_PF1(VSUAK)_PFA(AK)_PF2(PAG).pdf; https://doaj.org/toc/2249-782X; https://doaj.org/toc/0973-709X

    URL الوصول: https://doaj.org/article/6d349e0d3e9245d2a523f88e9a525ca6

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  2. 2
    Evaluation of patient’s satisfaction in the surgical units in a tertiary care public hospital

    المؤلفون: Astha Sarda, Lata N. Bhoir, Mrida Jhingan

    المصدر: International Journal of Medical Research and Review. 4:1079-1085

    مصطلحات موضوعية: Government, business.industry, Health care provider, media_common.quotation_subject, Medical care, Tertiary care, Nursing, Public hospital, Medicine, Quality (business), Obligation, business, Personal interview, media_common

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::0591c0535437b77c4ddc2078aef787bf
    https://doi.org/10.17511/ijmrr.2016.i06.36

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  3. 3
    Clinical phenotype and the lack of mutations in the CHRNG, CHRND, and CHRNA1 genes in two Indian families with Escobar syndrome

    المؤلفون: Srinivas G. Kodaganur, Vishwanath Kumble Bhat, Sagar J. Tontanahal, Astha Sarda, Mohd Hussain Shah, Arun Kumar

    المصدر: Clinical Dysmorphology. 22:54-58

    مصطلحات موضوعية: Male, Adolescent, DNA Mutational Analysis, India, Receptors, Nicotinic, Biology, medicine.disease_cause, Genetic analysis, Pathology and Forensic Medicine, Young Adult, Exon, medicine, Humans, Coding region, Abnormalities, Multiple, Genetic Predisposition to Disease, Receptors, Cholinergic, Gene, Genetics (clinical), Genetics, Mutation, Intron, Infant, Exons, General Medicine, Phenotype, Introns, Pedigree, genomic DNA, Genetic Loci, Child, Preschool, Pediatrics, Perinatology and Child Health, Skin Abnormalities, Female, Anatomy, Malignant Hyperthermia

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33521289111b9dbee7b8071e3202171a
    https://doi.org/10.1097/mcd.0b013e32835f9ac0

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  4. 4
    A homozygous mutation in TRIM36 causes autosomal recessive anencephaly in an Indian family

    المؤلفون: Nivedita Singh, Sagar J. Tontanahal, Vishwanath Kumble Bhat, Arun Kumar, Astha Sarda, K.V. Malini, Ankana Tiwari, Srinivas G. Kodaganur

    المصدر: Human molecular genetics. 26(6)

    مصطلحات موضوعية: 0301 basic medicine, Male, Mutant, India, Biology, medicine.disease_cause, 03 medical and health sciences, Fetus, Genetics, medicine, Missense mutation, Humans, Exome, Molecular Biology, Gene, Genetics (clinical), Mutation, Anencephaly, Neurogenesis, Homozygote, General Medicine, Transfection, Molecular biology, Pedigree, 030104 developmental biology, Neurulation, Female, Carrier Proteins, Cytokinesis

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99a1fc28ef305d66622615b83f270484
    https://pubmed.ncbi.nlm.nih.gov/28087737

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