Kagan-Hallet KS - Search Results

1

Tomaculous neuropathy: a clinical and electrophysiological study in patients with and without 1.5-Mb deletions in chromosome 17p11.2.

Amato AA, Gronseth GS, Callerame KJ, Kagan-Hallet KS, Bryan WW, Barohn RJ. Amato AA, et al. Among authors: kagan hallet ks. Muscle Nerve. 1996 Jan;19(1):16-22. doi: 10.1002/(SICI)1097-4598(199601)19:1<16::AID-MUS3>3.0.CO;2-B. Muscle Nerve. 1996. PMID: 8538664

2

The wide spectrum of myofibrillar myopathy suggests a multifactorial etiology and pathogenesis.

Amato AA, Kagan-Hallet K, Jackson CE, Lampkin S, Wolfe GI, Ferrante M, Bigio EH, Barohn RJ. Amato AA, et al. Neurology. 1998 Dec;51(6):1646-55. doi: 10.1212/wnl.51.6.1646. Neurology. 1998. PMID: 9855517

3

Neonatal nemaline myopathy with abundant intranuclear rods.

Barohn RJ, Jackson CE, Kagan-Hallet KS. Barohn RJ, et al. Among authors: kagan hallet ks. Neuromuscul Disord. 1994 Sep-Nov;4(5-6):513-20. doi: 10.1016/0960-8966(94)90092-2. Neuromuscul Disord. 1994. PMID: 7881297

4

Myofibrillar myopathy: no evidence of apoptosis by TUNEL.

Amato AA, Jackson CE, Lampkin S, Kagan-Hallet K. Amato AA, et al. Neurology. 1999 Mar 10;52(4):861-3. doi: 10.1212/wnl.52.4.861. Neurology. 1999. PMID: 10078743

5

Congenital ceroid-lipofuscinosis.

Barohn RJ, Dowd DC, Kagan-Hallet KS. Barohn RJ, et al. Among authors: kagan hallet ks. Pediatr Neurol. 1992 Jan-Feb;8(1):54-9. doi: 10.1016/0887-8994(92)90054-3. Pediatr Neurol. 1992. PMID: 1558577

6

Evaluation of neuromuscular symptoms in veterans of the Persian Gulf War.

Amato AA, McVey A, Cha C, Matthews EC, Jackson CE, Kleingunther R, Worley L, Cornman E, Kagan-Hallet K. Amato AA, et al. Neurology. 1997 Jan;48(1):4-12. doi: 10.1212/wnl.48.1.4. Neurology. 1997. PMID: 9008485

7

Anti-intercellular adhesion molecule-1 (ICAM-1) antibody treatment prevents central and peripheral nervous system disease in autoimmune-prone mice.

Brey RL, Amato AA, Kagan-Hallet K, Rhine CB, Stallworth CL. Brey RL, et al. Lupus. 1997;6(8):645-51. doi: 10.1177/096120339700600805. Lupus. 1997. PMID: 9364423

8

Loss of heterozygosity on chromosome 10 in human glioblastoma multiforme.

Fujimoto M, Fults DW, Thomas GA, Nakamura Y, Heilbrun MP, White R, Story JL, Naylor SL, Kagan-Hallet KS, Sheridan PJ. Fujimoto M, et al. Among authors: kagan hallet ks. Genomics. 1989 Feb;4(2):210-4. doi: 10.1016/0888-7543(89)90302-9. Genomics. 1989. PMID: 2544511

9

Mitochondrial myopathy presenting as temporomandibular dysfunction.

Van Sickels JE, Gruber AB, Kagan-Hallet KS, Dowd DC. Van Sickels JE, et al. J Oral Maxillofac Surg. 1987 Feb;45(2):168-72. doi: 10.1016/0278-2391(87)90408-3. J Oral Maxillofac Surg. 1987. PMID: 3468219

10

Poisoning from thallium.

Schwartz JG, Stuckey JH, Kunkel SP, Dowd DC, Kagan-Hallet KS. Schwartz JG, et al. Among authors: kagan hallet ks. Tex Med. 1988 Aug;84(8):46-8. Tex Med. 1988. PMID: 2845597 No abstract available.

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