Chang HW - Search Results

1

Dystrophinopathy in two young boys with exercise-induced cramps and myoglobinuria.

Minetti C, Tanji K, Chang HW, Medori R, Cordone G, DiMauro S, Bonilla E. Minetti C, et al. Among authors: chang hw. Eur J Pediatr. 1993 Oct;152(10):848-51. doi: 10.1007/BF02073385. Eur J Pediatr. 1993. PMID: 8223790

2

Dystrophin deficiency in young girls with sporadic myopathy and normal karyotype.

Minetti C, Chang HW, Medori R, Prelle A, Moggio M, Johnsen SD, Bonilla E. Minetti C, et al. Among authors: chang hw. Neurology. 1991 Aug;41(8):1288-92. doi: 10.1212/wnl.41.8.1288. Neurology. 1991. PMID: 1714059

3

Becker muscular dystrophy or spinal muscular atrophy?--Dystrophin studies resolve conflicting results of electromyography and muscle biopsy.

McDonald TD, Medori R, Younger DS, Chang HW, Minetti C, Uncini A, Bonilla E, Hays AP, Lovelace RE. McDonald TD, et al. Among authors: chang hw. Neuromuscul Disord. 1991;1(3):195-200. doi: 10.1016/0960-8966(91)90024-m. Neuromuscul Disord. 1991. PMID: 1822794

4

Partial dystrophin deficiency in monozygous twin carriers of the Duchenne gene discordant for clinical myopathy.

Bonilla E, Younger DS, Chang HW, Tantravahi U, Miranda AF, Medori R, DiMauro S, Warburton D, Rowland LP. Bonilla E, et al. Among authors: chang hw. Neurology. 1990 Aug;40(8):1267-70. doi: 10.1212/wnl.40.8.1267. Neurology. 1990. PMID: 2199849

5

Dystrophin in electric organ of Torpedo californica homologous to that in human muscle.

Chang HW, Bock E, Bonilla E. Chang HW, et al. J Biol Chem. 1989 Dec 15;264(35):20831-4. J Biol Chem. 1989. PMID: 2556382 Free article.

6

Normal and dystrophin-deficient muscle fibers in carriers of the gene for Duchenne muscular dystrophy.

Bonilla E, Schmidt B, Samitt CE, Miranda AF, Hays AP, de Oliveira AB, Chang HW, Servidei S, Ricci E, Younger DS, et al. Bonilla E, et al. Among authors: chang hw. Am J Pathol. 1988 Dec;133(3):440-5. Am J Pathol. 1988. PMID: 3059802 Free PMC article.

7

[Clinical,manifestations of the myopathies due to deletions/mutations of the dystrophin gene].

Bonilla E, Minetti C, Chang HW, Medori R, Cordone G, Di Mauro S. Bonilla E, et al. Among authors: chang hw. Minerva Pediatr. 1991 Mar;43(3):67-70. Minerva Pediatr. 1991. PMID: 1870528 Italian. No abstract available.

8

Phosphoglycerate kinase deficiency myopathy: biochemical and immunological studies of the mutant enzyme.

Bresolin N, Miranda A, Chang HW, Shanske S, DiMauro S. Bresolin N, et al. Among authors: chang hw. Muscle Nerve. 1984 Sep;7(7):542-51. doi: 10.1002/mus.880070705. Muscle Nerve. 1984. PMID: 6544372

9

Factors influencing the stability of isolated acetylcholine receptor from Torpedo californica.

Chang HW, Bock E. Chang HW, et al. Neurochem Int. 1980;2C:269-80. doi: 10.1016/0197-0186(80)90034-0. Neurochem Int. 1980. PMID: 20487793

10

Peak serum lactate as a robust predictor of imminent death in life-sustaining treatment decisions: A study of 73,927 patients.

Kim DJ, Kim HJ, Chang HW. Kim DJ, et al. Among authors: chang hw. Sci Prog. 2025 Jan-Mar;108(1):368504241311966. doi: 10.1177/00368504241311966. Sci Prog. 2025. PMID: 39763205 Free PMC article.

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