Bossen EH - Search Results

1

Clinical Studies in Non-chromosome 4-Linked Facioscapulohumeral Muscular Dystrophy.

Tim RW, Gilbert JR, Stajich JM, Rampersaud E, Viles KD, Tawil R, Padberg GW, Frants R, van der Maarel S, Bossen EH, Friedman AH, Pericak-Vance MA, Speer MC. Tim RW, et al. Among authors: bossen eh. J Clin Neuromuscul Dis. 2001 Sep;3(1):1-7. doi: 10.1097/00131402-200109000-00001. J Clin Neuromuscul Dis. 2001. PMID: 19078645

2

Recombinant human acid alpha-glucosidase enzyme therapy for infantile glycogen storage disease type II: results of a phase I/II clinical trial.

Amalfitano A, Bengur AR, Morse RP, Majure JM, Case LE, Veerling DL, Mackey J, Kishnani P, Smith W, McVie-Wylie A, Sullivan JA, Hoganson GE, Phillips JA 3rd, Schaefer GB, Charrow J, Ware RE, Bossen EH, Chen YT. Amalfitano A, et al. Among authors: bossen eh. Genet Med. 2001 Mar-Apr;3(2):132-8. Genet Med. 2001. PMID: 11286229 Free article. Clinical Trial.

3

Recurrent papules on the left upper extremity of a 50-year-old man.

Bettencourt MS, Burton CS, Prieto VG, Bossen EH, Shea CR. Bettencourt MS, et al. Among authors: bossen eh. Arch Dermatol. 2001 Mar;137(3):365-70. Arch Dermatol. 2001. PMID: 11255341 No abstract available.

4

Pathology quiz case 1. Hairy polyp.

Lansford CD, Bossen EH, Scher RL. Lansford CD, et al. Among authors: bossen eh. Arch Otolaryngol Head Neck Surg. 2003 Mar;129(3):369, 371. doi: 10.1001/archotol.129.3.369. Arch Otolaryngol Head Neck Surg. 2003. PMID: 12622554 No abstract available.

5

Characterization of pre- and post-treatment pathology after enzyme replacement therapy for Pompe disease.

Thurberg BL, Lynch Maloney C, Vaccaro C, Afonso K, Tsai AC, Bossen E, Kishnani PS, O'Callaghan M. Thurberg BL, et al. Lab Invest. 2006 Dec;86(12):1208-20. doi: 10.1038/labinvest.3700484. Epub 2006 Oct 30. Lab Invest. 2006. PMID: 17075580 Free article.

6

Chorionic villus ultrastructure in type II glycogen storage disease (Pompe's disease).

Hug G, Chuck G, Chen YT, Kay HH, Bossen EH. Hug G, et al. Among authors: bossen eh. N Engl J Med. 1991 Jan 31;324(5):342-3. doi: 10.1056/NEJM199101313240517. N Engl J Med. 1991. PMID: 1986298 No abstract available.

7

Mitochondrial myopathy with anemia, cardiomyopathy, and lactic acidosis: a distinct late onset mitochondrial disorder.

Van Hove JL, Shanske S, Ciacci F, Ballinger S, Shoffner JS, Wallace DC, Hanioka T, Folkers K, Bossen EH, Kussin PS, et al. Van Hove JL, et al. Among authors: bossen eh. Am J Med Genet. 1994 Jun 1;51(2):114-20. doi: 10.1002/ajmg.1320510207. Am J Med Genet. 1994. PMID: 8092186

8

Acute pancreatitis in an infant with lactic acidosis and a mutation at nucleotide 3243 in the mitochondrial DNA tRNALeu(UUR) gene.

Kishnani PS, Van Hove JL, Shoffner JS, Kaufman A, Bossen EH, Kahler SG. Kishnani PS, et al. Among authors: bossen eh. Eur J Pediatr. 1996 Oct;155(10):898-903. doi: 10.1007/BF02282842. Eur J Pediatr. 1996. PMID: 8891562

9

Oncocytic differentiation in intrahepatic biliary cystadenocarcinoma.

Wolf HK, Garcia JA, Bossen EH. Wolf HK, et al. Among authors: bossen eh. Mod Pathol. 1992 Nov;5(6):665-8. Mod Pathol. 1992. PMID: 1369804

10

Skeletal muscle microvasculature in the diagnosis of neuromuscular disease.

Buckley AF, Bossen EH. Buckley AF, et al. Among authors: bossen eh. J Neuropathol Exp Neurol. 2013 Oct;72(10):906-18. doi: 10.1097/NEN.0b013e3182a7f0b8. J Neuropathol Exp Neurol. 2013. PMID: 24042201 Review.

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