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Items: 10

1.

Metabolic Disorders in Iranian Children with Urolithiasis.

Mojtahedi SY, Abbasi A, Izadi A, Alavije FS, Fahimi D.

Maedica (Buchar). 2019 Sep;14(3):270-273. doi: 10.26574/maedica.2019.14.3.270.

2.

Association of bone mineral density with biochemical markers of bone turnover in hemodialysis children.

Hajizadeh N, Mehrkash M, Fahimi D, Qorbani M, Shafa N.

J Renal Inj Prev. 2016 Jul 27;5(4):174-8. doi: 10.15171/jrip.2016.37. eCollection 2016.

3.

A Comparison between Clinical and Metabolic Features of Renal Calyceal Microlithiasis and Overt Urolithiasis in Different Pediatric Age Groups.

Fahimi D, Habibi Zoham M, Sheikh M, Salabati M, Ghazanfari A, Firouzi M, Honarmand M.

Urol Int. 2016;96(1):91-8. doi: 10.1159/000441126. Epub 2015 Oct 21.

PMID:
26484860
4.

An estimation of steroid responsiveness of idiopathic nephrotic syndrome in Iranian children.

Madani A, Fahimi D, Taghaodi R, Mahjoob F, Hajizadeh N, Navabi B.

Iran J Pediatr. 2010 Jun;20(2):199-205.

5.

Comparison between fractional excretions of urea and sodium in children with acute kidney injury.

Fahimi D, Mohajeri S, Hajizadeh N, Madani A, Esfahani ST, Ataei N, Mohsseni P, Honarmand M.

Pediatr Nephrol. 2009 Dec;24(12):2409-12. doi: 10.1007/s00467-009-1271-1.

PMID:
19756765
6.

Absence of peroxisomes in mouse hepatocytes causes mitochondrial and ER abnormalities.

Dirkx R, Vanhorebeek I, Martens K, Schad A, Grabenbauer M, Fahimi D, Declercq P, Van Veldhoven PP, Baes M.

Hepatology. 2005 Apr;41(4):868-78.

PMID:
15732085
7.

Neuronal migration depends on intact peroxisomal function in brain and in extraneuronal tissues.

Janssen A, Gressens P, Grabenbauer M, Baumgart E, Schad A, Vanhorebeek I, Brouwers A, Declercq PE, Fahimi D, Evrard P, Schoonjans L, Collen D, Carmeliet P, Mannaerts G, Van Veldhoven P, Baes M.

J Neurosci. 2003 Oct 29;23(30):9732-41.

8.

Glomerular diseases in Iranian children: clinico-pathological correlations.

Madani A, Fahimi D, Esfehani ST, Mohsseni P, Atayee N, Ahmadi M, Elmi F, Haddadi M.

Pediatr Nephrol. 2003 Sep;18(9):925-8. Epub 2003 Jul 26.

PMID:
12898372
9.

A mouse model for Zellweger syndrome.

Baes M, Gressens P, Baumgart E, Carmeliet P, Casteels M, Fransen M, Evrard P, Fahimi D, Declercq PE, Collen D, van Veldhoven PP, Mannaerts GP.

Nat Genet. 1997 Sep;17(1):49-57.

PMID:
9288097

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