Gascon GG - Search Results

1

Phenotypic heterogeneity of spinal muscular atrophy mapping to chromosome 5q11.2-13.3 (SMA 5q).

Munsat TL, Skerry L, Korf B, Pober B, Schapira Y, Gascon GG, al-Rajeh SM, Dubowitz V, Davies K, Brzustowicz LM, et al. Munsat TL, et al. Among authors: gascon gg. Neurology. 1990 Dec;40(12):1831-6. doi: 10.1212/wnl.40.12.1831. Neurology. 1990. PMID: 2247230

2

Werdnig Hoffman's disease (spinal muscular atrophy type I): A clinical study of 25 Saudi nationals in Al-Khobar.

Al-Rajeh S, Bademosi O, Gascon GG, Stumpf D. Al-Rajeh S, et al. Among authors: gascon gg. Ann Saudi Med. 1992 Jan;12(1):67-71. doi: 10.5144/0256-4947.1992.67. Ann Saudi Med. 1992. PMID: 17589132 Free article.

3

Successful treatment of cherry red spot-myoclonus syndrome with 5-hydroxytryptophan.

Gascon G, Wallenberg B, Daif AK, Ozand P. Gascon G, et al. Ann Neurol. 1988 Sep;24(3):453-5. doi: 10.1002/ana.410240317. Ann Neurol. 1988. PMID: 3265864

4

Infantile CNS spongy degeneration--14 cases: clinical update.

Gascon GG, Ozand PT, Mahdi A, Jamil A, Haider A, Brismar J, al-Nasser M. Gascon GG, et al. Neurology. 1990 Dec;40(12):1876-82. doi: 10.1212/wnl.40.12.1876. Neurology. 1990. PMID: 2247237

5

Coincident neuraminidase and aspartoacylase deficiency associated with chromosome 9Q paracentric inversion in a Saudi family.

Gascon GG, Youssef NG, Subramanyam SB, Ozand PT. Gascon GG, et al. J Child Neurol. 1992 Apr;7 Suppl:S73-8. doi: 10.1177/08830738920070011111. J Child Neurol. 1992. PMID: 1588018

6

Congenital muscular dystrophy with abnormal radiographic myelin pattern.

Cook JD, Gascon GG, Haider A, Coates R, Stigsby B, Ozand PT, Banna M. Cook JD, et al. Among authors: gascon gg. J Child Neurol. 1992 Apr;7 Suppl:S51-63. doi: 10.1177/08830738920070010811. J Child Neurol. 1992. PMID: 1588016

7

Biopterin-dependent hyperphenylalaninemia due to deficiency of 6-pyruvoyl tetrahydropterin synthase.

al Aqeel A, Ozand PT, Gascon G, Nester M, al Nasser M, Brismar J, Blau N, Hughes H, Subramanyan SB, Reynolds CT. al Aqeel A, et al. Neurology. 1991 May;41(5):730-7. doi: 10.1212/wnl.41.5.730. Neurology. 1991. PMID: 2027491

8

Riyadh chromosome breakage syndrome: mental retardation with depigmentation of the skin and hair.

Ozand PT, Waghray M, Cook JD, Sheth K, Gascon GG. Ozand PT, et al. Among authors: gascon gg. J Child Neurol. 1992 Apr;7 Suppl:S79-82. doi: 10.1177/08830738920070011211. J Child Neurol. 1992. PMID: 1588019

9

Neurologic disorders in Saudi children.

Gascon GG. Gascon GG. Ann Saudi Med. 1993 Jan;13(1):91. doi: 10.5144/0256-4947.1993.91. Ann Saudi Med. 1993. PMID: 17588003 Free article. No abstract available.

10

Vigabatrin in medically resistant epilepsies - A preliminary experience with nine Saudi children.

Al Jarallah A, Gascon GG. Al Jarallah A, et al. Among authors: gascon gg. Ann Saudi Med. 1994 Mar;14(2):165-6. doi: 10.5144/0256-4947.1994.165. Ann Saudi Med. 1994. PMID: 17586879 Free article. No abstract available.

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