T32 GM082773/GM/NIGMS NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
2009	2
2010	3
2011	8
2012	3
2013	11
2014	13
2015	9
2016	12
2017	6
2018	5
2019	1
2020	2
2021	3
2022	1
2023	1
2024	0

1

Approach to the Management of Recently Diagnosed Inflammatory Bowel Disease Patients: A User's Guide for Adult and Pediatric Gastroenterologists.

Agrawal M, Spencer EA, Colombel JF, Ungaro RC. Agrawal M, et al. Gastroenterology. 2021 Jul;161(1):47-65. doi: 10.1053/j.gastro.2021.04.063. Epub 2021 Apr 30. Gastroenterology. 2021. PMID: 33940007 Free PMC article. Review.

2

The porphyrias: advances in diagnosis and treatment.

Balwani M, Desnick RJ. Balwani M, et al. Blood. 2012 Nov 29;120(23):4496-504. doi: 10.1182/blood-2012-05-423186. Epub 2012 Jul 12. Blood. 2012. PMID: 22791288 Free PMC article. Review.

3

Prospective investigation of FOXP1 syndrome.

Siper PM, De Rubeis S, Trelles MDP, Durkin A, Di Marino D, Muratet F, Frank Y, Lozano R, Eichler EE, Kelly M, Beighley J, Gerdts J, Wallace AS, Mefford HC, Bernier RA, Kolevzon A, Buxbaum JD. Siper PM, et al. Mol Autism. 2017 Oct 24;8:57. doi: 10.1186/s13229-017-0172-6. eCollection 2017. Mol Autism. 2017. PMID: 29090079 Free PMC article.

4

Implementation and utilization of genetic testing in personalized medicine.

Abul-Husn NS, Owusu Obeng A, Sanderson SC, Gottesman O, Scott SA. Abul-Husn NS, et al. Pharmgenomics Pers Med. 2014 Aug 13;7:227-40. doi: 10.2147/PGPM.S48887. eCollection 2014. Pharmgenomics Pers Med. 2014. PMID: 25206309 Free PMC article. Review.

5

Fragile X syndrome: A review of clinical management.

Lozano R, Azarang A, Wilaisakditipakorn T, Hagerman RJ. Lozano R, et al. Intractable Rare Dis Res. 2016 Aug;5(3):145-57. doi: 10.5582/irdr.2016.01048. Intractable Rare Dis Res. 2016. PMID: 27672537 Free PMC article. Review.

6

Liver transplantation for pediatric inherited metabolic disorders: Considerations for indications, complications, and perioperative management.

Oishi K, Arnon R, Wasserstein MP, Diaz GA. Oishi K, et al. Pediatr Transplant. 2016 Sep;20(6):756-69. doi: 10.1111/petr.12741. Epub 2016 Jun 21. Pediatr Transplant. 2016. PMID: 27329540 Free PMC article. Review.

7

Diverse and unselected adults with clinically relevant ACADS variants lack evidence of metabolic disease.

Breilyn MS, Kenny EE, Abul-Husn NS. Breilyn MS, et al. Mol Genet Metab. 2023 Jan;138(1):106971. doi: 10.1016/j.ymgme.2022.106971. Epub 2022 Dec 15. Mol Genet Metab. 2023. PMID: 36549199 Free PMC article.

8

Update on the Clinical, Radiographic, and Neurobehavioral Manifestations in FXTAS and FMR1 Premutation Carriers.

Hall DA, Robertson E, Shelton AL, Losh MC, Mila M, Moreno EG, Gomez-Anson B, Martínez-Cerdeño V, Grigsby J, Lozano R, Hagerman R, Maria LS, Berry-Kravis E, O'Keefe JA. Hall DA, et al. Cerebellum. 2016 Oct;15(5):578-86. doi: 10.1007/s12311-016-0799-4. Cerebellum. 2016. PMID: 27287737 Free PMC article. Review.

9

Acute Intermittent Porphyria in children: A case report and review of the literature.

Balwani M, Singh P, Seth A, Debnath EM, Naik H, Doheny D, Chen B, Yasuda M, Desnick RJ. Balwani M, et al. Mol Genet Metab. 2016 Dec;119(4):295-299. doi: 10.1016/j.ymgme.2016.10.005. Epub 2016 Oct 15. Mol Genet Metab. 2016. PMID: 27769855 Free PMC article. Review.

10

Aging in Fragile X Premutation Carriers.

Lozano R, Saito N, Reed D, Eldeeb M, Schneider A, Hessl D, Tassone F, Beckett L, Hagerman R. Lozano R, et al. Cerebellum. 2016 Oct;15(5):587-94. doi: 10.1007/s12311-016-0805-x. Cerebellum. 2016. PMID: 27334385 Free PMC article. Clinical Trial.

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