Tawam Hospital View Homepage


Ontology type: grid:Healthcare  | foaf:Organization     


Publications in SciGraph latest 20 shown

  • 2019-12 Trefoil factors peptide-3 is associated with residual invasive breast carcinoma following neoadjuvant chemotherapy in BMC CANCER
  • 2019-12 De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndrome in GENOME MEDICINE
  • 2019-12 Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndrome in GENOME MEDICINE
  • 2019-03-07 Comparison of perceptions of unmet supportive care needs between cancer patients and their oncologists in SUPPORTIVE CARE IN CANCER
  • 2018-12 Can untreated PKU patients escape from intellectual disability? A systematic review in ORPHANET JOURNAL OF RARE DISEASES
  • 2018-12 DNA methylation and repressive H3K9 and H3K27 trimethylation in the promoter regions of PD-1, CTLA-4, TIM-3, LAG-3, TIGIT, and PD-L1 genes in human primary breast cancer in CLINICAL EPIGENETICS
  • 2018-12 Compound heterozygous variants in the multiple PDZ domain protein (MPDZ) cause a case of mild non-progressive communicating hydrocephalus in BMC MEDICAL GENETICS
  • 2018-10 Re-induction chemotherapy using FLAG–mitoxantrone for adult patients with relapsed acute leukemia: a single-center experience from United Arab Emirates in INTERNATIONAL JOURNAL OF HEMATOLOGY
  • 2018-09 Management of acromegaly: an exploratory survey of physicians from the Middle East and North Africa in HORMONES
  • 2018-08 Contribution of Type 2 Diabetes Mellitus to Subclinical Atherosclerosis in Subjects with Morbid Obesity in OBESITY SURGERY
  • 2018-08 Acquired thrombotic thrombocytopenic purpura with isolated CFHR3/1 deletion—rapid remission following complement blockade in PEDIATRIC NEPHROLOGY
  • 2018-01 Correction to: Expanding the genetic heterogeneity of intellectual disability in HUMAN GENETICS
  • 2017-12 Knowledge, attitudes, and practices of pediatricians on infantile colic in the Middle East and North Africa region in BMC PEDIATRICS
  • 2017-12 De novo chromosome 7q36.1q36.2 triplication in a child with developmental delay, growth failure, distinctive facial features, and multiple congenital anomalies: a case report in BMC MEDICAL GENETICS
  • 2017-12 Discriminating between positional and non-positional obstructive sleep apnea using some clinical characteristics in SLEEP AND BREATHING
  • 2017-12 Disseminated Bacillus Calmette-Guérin (BCG) infections in infants with immunodeficiency in BMC RESEARCH NOTES
  • 2017-12 17q23.2q23.3 de novo duplication in association with speech and language disorder, learning difficulties, incoordination, motor skill impairment, and behavioral disturbances: a case report in BMC MEDICAL GENETICS
  • 2017-11 Oral D-galactose supplementation in PGM1-CDG in GENETICS IN MEDICINE
  • 2017-11 Expanding the genetic heterogeneity of intellectual disability in HUMAN GENETICS
  • 2017-08 Erratum to: Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic features in HUMAN GENETICS
  • JSON-LD is the canonical representation for SciGraph data.

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    Download the RDF metadata as:  json-ld nt turtle xml License info

    HOW TO GET THIS DATA PROGRAMMATICALLY:

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    curl -H 'Accept: application/ld+json' 'https://www.grid.ac/institutes/grid.416924.c'

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    RDF/XML is a standard XML format for linked data.

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    This table displays all metadata directly associated to this object as RDF triples.

    55 TRIPLES      9 PREDICATES      10 URIs      4 LITERALS

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