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Intracranial hemorrhage in primary immune thrombocytopenia (ITP): 20 years' experience in pediatrics.
Eur J Pediatr. 2021 May;180(5):1545-1552. doi: 10.1007/s00431-020-03923-x. Epub 2021 Jan 15.
Eur J Pediatr. 2021.
PMID: 33452569
Intracranial haemorrhage associated with Vitamin K deficiency in Egyptian infants.
Elalfy M, Eltonbary K, Elalfy O, Gadallah M, Zidan A, Abdel-Hady H.
Elalfy M, et al.
Acta Paediatr. 2021 Nov;110(11):2937-2943. doi: 10.1111/apa.16011. Epub 2021 Jul 8.
Acta Paediatr. 2021.
PMID: 34196053
Review.
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Management of children with glucose-6-phosphate dehydrogenase deficiency presenting with acute haemolytic crisis during the SARs-COV-2 pandemic.
Elalfy M, Adly A, Eltonbary K, Elghamry I, Elalfy O, Maebid M, Elsayh K, Elsayed HN, El Ekiaby M.
Elalfy M, et al.
Vox Sang. 2022 Jan;117(1):80-86. doi: 10.1111/vox.13123. Epub 2021 Jun 8.
Vox Sang. 2022.
PMID: 34105166
Free PMC article.
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Congenital hyperinsulinism: management and outcome, a single tertiary centre experience.
El Tonbary K, Robinson P, Banerjee I, Shaikh MG.
El Tonbary K, et al.
Eur J Pediatr. 2020 Jun;179(6):947-952. doi: 10.1007/s00431-020-03581-z. Epub 2020 Jan 30.
Eur J Pediatr. 2020.
PMID: 32002613
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Phenotypic severity of homozygous GCK mutations causing neonatal or childhood-onset diabetes is primarily mediated through effects on protein stability.
Raimondo A, Chakera AJ, Thomsen SK, Colclough K, Barrett A, De Franco E, Chatelas A, Demirbilek H, Akcay T, Alawneh H; International NDM Consortium; Flanagan SE, Van De Bunt M, Hattersley AT, Gloyn AL, Ellard S; International NDM Consortium.
Raimondo A, et al.
Hum Mol Genet. 2014 Dec 15;23(24):6432-40. doi: 10.1093/hmg/ddu360. Epub 2014 Jul 11.
Hum Mol Genet. 2014.
PMID: 25015100
Free PMC article.
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