Souza SC - Search Results

1

Usefulness of MLPA in the detection of SHOX deletions.

Funari MF, Jorge AA, Souza SC, Billerbeck AE, Arnhold IJ, Mendonca BB, Nishi MY. Funari MF, et al. Among authors: souza sc. Eur J Med Genet. 2010 Sep-Oct;53(5):234-8. doi: 10.1016/j.ejmg.2010.06.001. Epub 2010 Jun 9. Eur J Med Genet. 2010. PMID: 20538086 Free article.

2

SHOX mutations in idiopathic short stature and Leri-Weill dyschondrosteosis: frequency and phenotypic variability.

Jorge AA, Souza SC, Nishi MY, Billerbeck AE, Libório DC, Kim CA, Arnhold IJ, Mendonca BB. Jorge AA, et al. Among authors: souza sc. Clin Endocrinol (Oxf). 2007 Jan;66(1):130-5. doi: 10.1111/j.1365-2265.2006.02698.x. Clin Endocrinol (Oxf). 2007. PMID: 17201812

3

[Short stature caused by SHOX gene haploinsufficiency: from diagnosis to treatment].

Jorge AA, Nishi MY, Funari MF, Souza SC, Arnhold IJ, Mendonça BB. Jorge AA, et al. Among authors: souza sc. Arq Bras Endocrinol Metabol. 2008 Jul;52(5):765-73. doi: 10.1590/s0004-27302008000500008. Arq Bras Endocrinol Metabol. 2008. PMID: 18797583 Review. Portuguese.

4

Analysis of the PTPN11 gene in idiopathic short stature children and Noonan syndrome patients.

Ferreira LV, Souza SC, Montenegro LR, Malaquias AC, Arnhold IJ, Mendonca BB, Jorge AA. Ferreira LV, et al. Among authors: souza sc. Clin Endocrinol (Oxf). 2008 Sep;69(3):426-31. doi: 10.1111/j.1365-2265.2008.03234.x. Epub 2008 Mar 10. Clin Endocrinol (Oxf). 2008. PMID: 18331608

5

Poor reproducibility of IGF-I and IGF binding protein-3 generation test in children with short stature and normal coding region of the GH receptor gene.

Jorge AA, Souza SC, Arnhold IJ, Mendonca BB. Jorge AA, et al. Among authors: souza sc. J Clin Endocrinol Metab. 2002 Feb;87(2):469-72. doi: 10.1210/jcem.87.2.8191. J Clin Endocrinol Metab. 2002. PMID: 11836270

6

[Noonan syndrome: from phenotype to growth hormone therapy].

Malaquias AC, Ferreira LV, Souza SC, Arnhold IJ, Mendonça BB, Jorge AA. Malaquias AC, et al. Among authors: souza sc. Arq Bras Endocrinol Metabol. 2008 Jul;52(5):800-8. doi: 10.1590/s0004-27302008000500012. Arq Bras Endocrinol Metabol. 2008. PMID: 18797587 Review. Portuguese.

7

The first homozygous mutation (S226I) in the highly-conserved WSXWS-like motif of the GH receptor causing Laron syndrome: supression of GH secretion by GnRH analogue therapy not restored by dihydrotestosterone administration.

Jorge AA, Souza SC, Arnhold IJ, Mendonca BB. Jorge AA, et al. Among authors: souza sc. Clin Endocrinol (Oxf). 2004 Jan;60(1):36-40. doi: 10.1111/j.1365-2265.2004.01930.x. Clin Endocrinol (Oxf). 2004. PMID: 14678285

8

[Tolerance of the oral clonidine test in 180 patients: efficacy of the volemic expantion in controlling arterial hypotension].

Marui S, Oliveira CH, Souza SC, Berger K, Khawali C, Hauache OM, Maciel RM, Vieira JG. Marui S, et al. Among authors: souza sc. Arq Bras Endocrinol Metabol. 2005 Aug;49(4):510-5. doi: 10.1590/s0004-27302005000400007. Epub 2005 Oct 19. Arq Bras Endocrinol Metabol. 2005. PMID: 16358078 Portuguese.

9

Using telemedicine and virtual healthcare to improve clinical follow-up for survivors of sexual assault and intimate partner violence: a 7-year investigation of emergency department cases.

Fagen J, Talarico R, Mercier O, Horth C, Souza SCS, Muldoon KA, Sampsel K. Fagen J, et al. Among authors: souza scs. CJEM. 2025 Jan 6. doi: 10.1007/s43678-024-00783-4. Online ahead of print. CJEM. 2025. PMID: 39762498

10

Isolated Vertical Gaze Palsy due to Unilateral Rostral Midbrain Stroke.

Urbano JCC, de Souza SC, Lopes CCB, Silva GD, Studart-Neto A, Freua F, Comerlatti LR. Urbano JCC, et al. Among authors: de souza sc. J Neuroophthalmol. 2024 Nov 7. doi: 10.1097/WNO.0000000000002281. Online ahead of print. J Neuroophthalmol. 2024. PMID: 39508799 No abstract available.

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