Jorge Sales Marques - Search Results

Year	Number of Results
2006	1
2008	1
2009	1
2012	1
2013	2
2014	2
2015	4
2019	1
2022	1
2024	0

1

The Clinical Management of Pompe Disease: A Pediatric Perspective.

Marques JS. Marques JS. Children (Basel). 2022 Sep 16;9(9):1404. doi: 10.3390/children9091404. Children (Basel). 2022. PMID: 36138713 Free PMC article. Review.

2

Visual Diagnosis: Large Mass with Ulceration over the Right Shoulder.

Amaral V, Tong J, Chow KC, Sales Marques J. Amaral V, et al. Among authors: sales marques j. Pediatr Rev. 2019 Aug;40(8):e28-e31. doi: 10.1542/pir.2017-0073. Pediatr Rev. 2019. PMID: 31371642 No abstract available.

3

Visual diagnosis: 8-day-old hypotonic newborn with sparse hair.

Marques JS, Mateus M, Torres T, Santos H, Real MV, Santos F. Marques JS, et al. Pediatr Rev. 2014 Nov;35(11):e53-6. doi: 10.1542/pir.35-11-e53. Pediatr Rev. 2014. PMID: 25361912

4

Growth hormone deficiency in a patient with mitochondrial disease.

Rocha V, Rocha D, Santos H, Sales Marques J. Rocha V, et al. Among authors: sales marques j. J Pediatr Endocrinol Metab. 2015 Sep;28(9-10):1003-4. doi: 10.1515/jpem-2014-0315. J Pediatr Endocrinol Metab. 2015. PMID: 25781523

5

Association of Turner Syndrome and Growth Hormone Deficiency: A Review.

Marques JS, Aires S. Marques JS, et al. Pediatr Endocrinol Rev. 2015 Sep;13(1):455-7. Pediatr Endocrinol Rev. 2015. PMID: 26540761

6

Neurofibromatosis Type 1: A Novel NF1 Mutation Associated with Mitochondrial Complex I Deficiency.

Domingues S, Isidoro L, Rocha D, Sales Marques J. Domingues S, et al. Among authors: sales marques j. Case Rep Genet. 2014;2014:423071. doi: 10.1155/2014/423071. Epub 2014 Mar 4. Case Rep Genet. 2014. PMID: 24711935 Free PMC article.

7

Index of suspicion.

Luck RP, Maggiori L, Poujade O, Ata T, Chouillard E, Marques JS, Garrido A, Real MV, Santos H, Alvares S. Luck RP, et al. Among authors: marques js. Pediatr Rev. 2006 Jul;27(7):271-7. doi: 10.1542/pir.27-7-271. Pediatr Rev. 2006. PMID: 16815996 No abstract available.

8

Identification of maternal uniparental isodisomy of chromosome 10 in a patient with mitochondrial DNA depletion syndrome.

Nogueira C, Marques JS, Nesti C, Azevedo L, Di Lullo M, Meschini MC, Orlacchio A, Santorelli FM, Vilarinho L. Nogueira C, et al. Among authors: marques js. Mol Genet Metab. 2013 Dec;110(4):493-4. doi: 10.1016/j.ymgme.2013.09.010. Epub 2013 Sep 25. Mol Genet Metab. 2013. PMID: 24148156 No abstract available.

9

Trichorhinophalangeal Syndrome Type I: A Patient with Two Novel and Different Mutations in the TRPS1 Gene.

Dias C, Isidoro L, Santos M, Santos H, Marques JS. Dias C, et al. Among authors: marques js. Case Rep Genet. 2013;2013:748057. doi: 10.1155/2013/748057. Epub 2013 Apr 17. Case Rep Genet. 2013. PMID: 23691375 Free PMC article.

10

European multicentre study in children born small for gestational age with persistent short stature: comparison of continuous and discontinuous growth hormone treatment regimens.

Phillip M, Lebenthal Y, Lebl J, Zuckerman-Levin N, Korpal-Szczyrska M, Marques JS, Steensberg A, Jons K, Kappelgaard AM, Ibanez L; European Norditropin SGA Study Group. Phillip M, et al. Among authors: marques js. Horm Res. 2009 Jan;71(1):52-9. doi: 10.1159/000173742. Epub 2008 Nov 27. Horm Res. 2009. PMID: 19039237 Clinical Trial.

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