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PUBMED FOR HANDHELDS

Journal Abstract Search


152 related items for PubMed ID: 35733479

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  • 8. Severe holocord syrinx in a child with megalencephaly-capillary malformation syndrome.
    Segal D, Heary RF, Sabharwal S, Barry MT, Ming X.
    J Neurosurg Pediatr; 2016 Jul; 18(1):79-82. PubMed ID: 27035547
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  • 9. The utility of cerebrospinal fluid-derived cell-free DNA in molecular diagnostics for the PIK3CA-related megalencephaly-capillary malformation (MCAP) syndrome: a case report.
    Chen WL, Pao E, Owens J, Glass I, Pritchard C, Shirts BH, Lockwood C, Mirzaa GM.
    Cold Spring Harb Mol Case Stud; 2022 Apr; 8(3):. PubMed ID: 35483878
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  • 13. Clinical and neuroimaging findings in 33 patients with MCAP syndrome: A survey to evaluate relevant endpoints for future clinical trials.
    Garde A, Guibaud L, Goldenberg A, Petit F, Dard R, Roume J, Mazereeuw-Hautier J, Chassaing N, Lacombe D, Morice-Picard F, Toutain A, Arpin S, Boccara O, Touraine R, Blanchet P, Coubes C, Willems M, Pinson L, Van Kien PK, Chiaverini C, Giuliano F, Alessandri JL, Mathieu-Dramard M, Morin G, Bursztejn AC, Mignot C, Doummar D, Di Rocco F, Cornaton J, Nicolas C, Gautier E, Luu M, Bardou M, Sorlin A, Philippe C, Edery P, Rossi M, Carmignac V, Thauvin-Robinet C, Vabres P, Faivre L.
    Clin Genet; 2021 May; 99(5):650-661. PubMed ID: 33415748
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  • 17. One of the First Cases with PIK3CA-related Overgrowth Spectrum (PROS) in Saudi Arabia: A Case Report and Literature Review.
    Alsaedi SA, Qurashi O, Bajunaid M, Altalhi AA, Shawli AM.
    Cureus; 2020 Jan 07; 12(1):e6586. PubMed ID: 31929958
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