Guarini L - Search Results

1

Rare Presentation of Adrenocortical Carcinoma in a 4-Month-Old Boy.

Malhotra S, Waikar AR, Singh P, Guarini L, Jacobson-Dickman E, Motaghedi R, Kazachkova I. Malhotra S, et al. Among authors: guarini l. World J Oncol. 2017 Jun;8(3):81-85. doi: 10.14740/wjon1036w. Epub 2017 Jun 9. World J Oncol. 2017. PMID: 29147440 Free PMC article.

2

Immunoproliferative small intestinal disease in a 16-year-old boy presenting as severe malabsorption with excellent response to tetracycline treatment.

Zamir A, Parasher G, Moukarzel AA, Guarini L, Zeien L, Feldman F. Zamir A, et al. Among authors: guarini l. J Clin Gastroenterol. 1998 Jul;27(1):85-9. doi: 10.1097/00004836-199807000-00020. J Clin Gastroenterol. 1998. PMID: 9706780

3

Sickle cell anemia: severe ischemic colitis responding to conservative management.

Moukarzel AA, Rajaram M, Sundeep A, Guarini L, Feldman F. Moukarzel AA, et al. Among authors: guarini l. Clin Pediatr (Phila). 2000 Apr;39(4):241-3. doi: 10.1177/000992280003900409. Clin Pediatr (Phila). 2000. PMID: 10791138 No abstract available.

4

Intravenous immunoglobulin treatment of congenital parvovirus B19 induced anemia - a case report.

Aronson ST, Celiker MY, Guarini L, Agha R. Aronson ST, et al. Among authors: guarini l. Matern Health Neonatol Perinatol. 2023 Aug 7;9(1):10. doi: 10.1186/s40748-023-00164-2. Matern Health Neonatol Perinatol. 2023. PMID: 37544998 Free PMC article.

5

Asymptomatic Retinal Vein Occlusion in a 13-Year-Old With Heterozygous Deletion of the PMP22 Gene and a Diagnosis of Hereditary Neuropathy With Liability to Pressure Palsies.

Saffra NA, Emborgo TS, Laureta EC, Kirsch DS, Guarini L. Saffra NA, et al. Among authors: guarini l. J Neuroophthalmol. 2022 Mar 1;42(1):e367-e370. doi: 10.1097/WNO.0000000000001233. Epub 2021 Apr 14. J Neuroophthalmol. 2022. PMID: 33870946 No abstract available.

6

Silent infarction as a risk factor for overt stroke in children with sickle cell anemia: a report from the Cooperative Study of Sickle Cell Disease.

Miller ST, Macklin EA, Pegelow CH, Kinney TR, Sleeper LA, Bello JA, DeWitt LD, Gallagher DM, Guarini L, Moser FG, Ohene-Frempong K, Sanchez N, Vichinsky EP, Wang WC, Wethers DL, Younkin DP, Zimmerman RA, DeBaun MR; Cooperative Study of Sickle Cell Disease. Miller ST, et al. Among authors: guarini l. J Pediatr. 2001 Sep;139(3):385-90. doi: 10.1067/mpd.2001.117580. J Pediatr. 2001. PMID: 11562618

7

Neuropsychologic performance in school-aged children with sickle cell disease: a report from the Cooperative Study of Sickle Cell Disease.

Wang W, Enos L, Gallagher D, Thompson R, Guarini L, Vichinsky E, Wright E, Zimmerman R, Armstrong FD; Cooperative Study of Sickle Cell Disease. Wang W, et al. Among authors: guarini l. J Pediatr. 2001 Sep;139(3):391-7. doi: 10.1067/mpd.2001.116935. J Pediatr. 2001. PMID: 11562619

8

Longitudinal changes in brain magnetic resonance imaging findings in children with sickle cell disease.

Pegelow CH, Macklin EA, Moser FG, Wang WC, Bello JA, Miller ST, Vichinsky EP, DeBaun MR, Guarini L, Zimmerman RA, Younkin DP, Gallagher DM, Kinney TR. Pegelow CH, et al. Among authors: guarini l. Blood. 2002 Apr 15;99(8):3014-8. doi: 10.1182/blood.v99.8.3014. Blood. 2002. PMID: 11929794 Free article.

9

Managing incidentally diagnosed isolated factor VII deficiency perioperatively: a brief expert consensus report.

Sheth S, Soff G, Mitchell B, Green D, Kaicker S, Fireman F, Tugal O, Guarini L, Giardina P, Aledort L. Sheth S, et al. Among authors: guarini l. Expert Rev Hematol. 2012 Feb;5(1):47-50. doi: 10.1586/ehm.11.76. Expert Rev Hematol. 2012. PMID: 22272705

10

Hydroxyurea in congenital erythropoietic porphyria.

Guarini L, Piomelli S, Poh-Fitzpatrick MB. Guarini L, et al. N Engl J Med. 1994 Apr 14;330(15):1091-2. doi: 10.1056/NEJM199404143301519. N Engl J Med. 1994. PMID: 8127351 No abstract available.

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