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20 results on '"Al-Saif, H"'

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1. Association of Variants in the SPTLC1 Gene with Juvenile Amyotrophic Lateral Sclerosis

2. Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis

3. Mutations in the SPTLC1 gene are a cause of juvenile amyotrophic lateral sclerosis that may be amenable to serine supplementation

6. Efficacy and safety of short-pulse erbium: Yttrium aluminum garnet laser treatment of Becker's nevus in Saudi patients: A pilot study.

7. Co-occurring Usher syndrome Type 1 and Renal Failure.

8. De novo variants in DENND5B cause a neurodevelopmental disorder.

9. Unveiling the crucial neuronal role of the proteasomal ATPase subunit gene PSMC5 in neurodevelopmental proteasomopathies.

10. Hereditary motor and sensory neuropathy type VIA with optic nerve pallor in two sisters with pathologic myopia: a case series and review.

11. A New Case and Comprehensive Review of the Ophthalmic Manifestations of 172 Individuals With Branchio-Oculo-Facial Syndrome.

12. Ophthalmologic and facial abnormalities of Nicolaides-Baraitser syndrome.

13. Ophthalmic abnormalities in Wieacker-Wolff syndrome.

14. Eye and ocular adnexa manifestations of MED12 -related disorders.

15. Eye, Ocular Adnexa, and Facial Manifestations of Tetrasomy 18p.

16. A Chromosomal Deletion and New Frameshift Mutation Cause ARSACS in an African-American.

17. A Rare Case of Unilateral Morning Glory Disc Anomaly in a Patient with Turner Syndrome: Report and Review of Posterior Segment Associations.

18. Multiloculated Cavitary Primary Pulmonary Hodgkin Lymphoma: Case Series.

19. Efficacy and safety of short-pulse erbium: Yttrium aluminum garnet laser treatment of Becker's nevus in Saudi patients: A pilot study.

20. Communicability of H1N1 and seasonal influenza among household contacts of cases in large families.

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