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Articles published in Arch Pediatr

Retrieve available abstracts of 8 articles:
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Single Articles

    August 2022
  1. MINARY K, Tanne C, Kwon T, Faudeux C, et al
    Outbreak of hemolytic uremic syndrome with unusually severe clinical presentation caused by Shiga toxin-producing Escherichia coli O26:H11 in France.
    Arch Pediatr. 2022;29:448-452.
    PubMed     Abstract available

    October 2021
  2. HEILBRONNER C, Grimaud M, Oualha M, Sommet J, et al
    Therapeutic approach to pediatric patients with acute chest syndrome: national multicenter survey of non invasive ventilation (NIV) and transfusion.
    Arch Pediatr. 2021;28:559-566.
    PubMed     Abstract available

    February 2021
  3. TEZOL O, Unal S
    Anxiety level and clinical course of patients with sickle cell disease during the COVID-19 outbreak.
    Arch Pediatr. 2021;28:136-140.
    PubMed     Abstract available

    January 2021
  4. PONDROM M, Monpoux F, Rocher F, Gastaut N, et al
    Tolerance induction to deferasirox in a child with transfusion-dependent beta thalassemia.
    Arch Pediatr. 2021;28:101-103.
    PubMed     Abstract available

    September 2020
  5. LEMOINE A, Tounian P
    Childhood anemia and iron deficiency in sub-Saharan Africa - risk factors and prevention: A review.
    Arch Pediatr. 2020 Sep 16. pii: S0929-693X(20)30191.
    PubMed     Abstract available

    November 2019
  6. REMION J, Pluchart C
    Targeted screening failures in neonates with sickle cell disease in metropolitan France from 2005 to 2017: Number of cases, failure circumstances and health at diagnosis.
    Arch Pediatr. 2019 Nov 1. pii: S0929-693X(19)30155.

    October 2019
  7. NEVEU J, Perelman S, Suisse G, Monpoux F, et al
    Severe hyperhomocysteinemia and peripheral neuropathy as side effects of nitrous oxide in two patients with sickle cell disease.
    Arch Pediatr. 2019;26:419-421.
    PubMed     Abstract available

    July 2019
  8. BEN FREDJ D, Barro C, Joly P, Thomassin N, et al
    Transient liver injury and severe neonatal cholestasis in infant with glucose-6-phosphate dehydrogenase deficiency due to a new mutation.
    Arch Pediatr. 2019 Jul 2. pii: S0929-693X(19)30093.
    PubMed     Abstract available

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