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Autosomal-Recessive Mutations in SLC34A1 Encoding Sodium-Phosphate Cotransporter 2A Cause Idiopathic Infantile Hypercalcemia.
J Am Soc Nephrol. 2016 Feb;27(2):604-14. doi: 10.1681/ASN.2014101025. Epub 2015 Jun 5.
J Am Soc Nephrol. 2016.
PMID: 26047794
Free PMC article.
Acute lymphoblastic leukaemia in a child with systemic lupus erythematosus.
Gokce M, Bulus D, Bilginer Y, Gumruk F, Besbas N, Cetin M.
Gokce M, et al. Among authors: bulus d.
Lupus. 2012 Jul;21(8):910-3. doi: 10.1177/0961203312436859. Epub 2012 Feb 13.
Lupus. 2012.
PMID: 22331193
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Clinical, biochemical and genetic features with nonclassical 21-hydroxylase deficiency and final height.
Savaş-Erdeve Ş, Çetinkaya S, Abalı ZY, Poyrazoğlu Ş, Baş F, Berberoğlu M, Sıklar Z, Korkmaz Ö, Buluş D, Akbaş ED, Güran T, Böber E, Akın O, Yılmaz GC, Aycan Z.
Savaş-Erdeve Ş, et al. Among authors: bulus d.
J Pediatr Endocrinol Metab. 2017 Jul 26;30(7):759-766. doi: 10.1515/jpem-2017-0088.
J Pediatr Endocrinol Metab. 2017.
PMID: 28672743
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Low 25-hydroxyvitamin D level is not an independent risk factor for hepatosteatosis in obese children.
Sezer OB, Buluş D, Hızlı Ş, Andıran N, Yılmaz D, Ramadan SU.
Sezer OB, et al. Among authors: bulus d.
J Pediatr Endocrinol Metab. 2016 Jul 1;29(7):783-8. doi: 10.1515/jpem-2015-0426.
J Pediatr Endocrinol Metab. 2016.
PMID: 27089408
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Hypophosphatemic rickets caused by a novel splice donor site mutation and activation of two cryptic splice donor sites in the PHEX gene.
Zou M, Buluş D, Al-Rijjal RA, Andıran N, BinEssa H, Kattan WE, Meyer B, Shi Y.
Zou M, et al. Among authors: bulus d.
J Pediatr Endocrinol Metab. 2015 Jan;28(1-2):211-6. doi: 10.1515/jpem-2014-0103.
J Pediatr Endocrinol Metab. 2015.
PMID: 25153221
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Central corneal thickness in children with diabetes.
Akinci A, Bulus D, Aycan Z, Oner O.
Akinci A, et al. Among authors: bulus d.
J Refract Surg. 2009 Nov;25(11):1041-4. doi: 10.3928/1081597X-20090617-04. Epub 2009 Nov 13.
J Refract Surg. 2009.
PMID: 19921774
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