Whiteman DA - Search Results

1

Diagnosis and management of defects of mitochondrial beta-oxidation.

Vockley J, Singh RH, Whiteman DA. Vockley J, et al. Among authors: whiteman da. Curr Opin Clin Nutr Metab Care. 2002 Nov;5(6):601-9. doi: 10.1097/00075197-200211000-00002. Curr Opin Clin Nutr Metab Care. 2002. PMID: 12394635 Review.

2

Defects of mitochondrial beta-oxidation: a growing group of disorders.

Vockley J, Whiteman DA. Vockley J, et al. Among authors: whiteman da. Neuromuscul Disord. 2002 Mar;12(3):235-46. doi: 10.1016/s0960-8966(01)00308-x. Neuromuscul Disord. 2002. PMID: 11801395 Review.

3

Primer on medical genomics. Part VIII: Essentials of medical genetics for the practicing physician.

Ensenauer RE, Reinke SS, Ackerman MJ, Tester DJ, Whiteman DA, Tefferi A. Ensenauer RE, et al. Among authors: whiteman da. Mayo Clin Proc. 2003 Jul;78(7):846-57. doi: 10.4065/78.7.846. Mayo Clin Proc. 2003. PMID: 12839081 Review.

4

Primer on medical genomics part II: Background principles and methods in molecular genetics.

Tefferi A, Wieben ED, Dewald GW, Whiteman DA, Bernard ME, Spelsberg TC. Tefferi A, et al. Among authors: whiteman da. Mayo Clin Proc. 2002 Aug;77(8):785-808. doi: 10.4065/77.8.785. Mayo Clin Proc. 2002. PMID: 12173714 Review.

5

Primer on medical genomics part I: History of genetics and sequencing of the human genome.

Lorentz CP, Wieben ED, Tefferi A, Whiteman DA, Dewald GW. Lorentz CP, et al. Among authors: whiteman da. Mayo Clin Proc. 2002 Aug;77(8):773-82. doi: 10.4065/77.8.773. Mayo Clin Proc. 2002. PMID: 12173713

6

Ehlers-Danlos syndrome type IV and a novel mutation of the type III procollagen gene as a cause of abdominal apoplexy.

Hassan I, Rasmussen TE, Schwarze U, Rose PS, Whiteman DA, Gloviczki P. Hassan I, et al. Among authors: whiteman da. Mayo Clin Proc. 2002 Aug;77(8):861-3. doi: 10.4065/77.8.861. Mayo Clin Proc. 2002. PMID: 12173720

7

Hypoglycinaemia and psychomotor delay in a child with xeroderma pigmentosum.

Quackenbush EJ, Kraemer KH, Gahl WA, Schirch V, Whiteman DA, Levine K, Levy HL. Quackenbush EJ, et al. Among authors: whiteman da. J Inherit Metab Dis. 1999 Dec;22(8):915-24. doi: 10.1023/a:1005691424004. J Inherit Metab Dis. 1999. PMID: 10604143

8

Limb anomalies in DiGeorge and CHARGE syndromes.

Prasad C, Quackenbush EJ, Whiteman D, Korf B. Prasad C, et al. Am J Med Genet. 1997 Jan 20;68(2):179-81. doi: 10.1002/(sici)1096-8628(19970120)68:2<179::aid-ajmg11>3.0.co;2-r. Am J Med Genet. 1997. PMID: 9028454

9

Cerebrovascular complications in Ehlers-Danlos syndrome type IV.

North KN, Whiteman DA, Pepin MG, Byers PH. North KN, et al. Among authors: whiteman da. Ann Neurol. 1995 Dec;38(6):960-4. doi: 10.1002/ana.410380620. Ann Neurol. 1995. PMID: 8526472 Review.

10

Molecular bases of hearing loss in multi-systemic mitochondrial cytopathy.

Scaglia F, Hsu CH, Kwon H, Bai RK, Perng CL, Chang HM, Dai P, Smith EO, Whiteman DA, Feigenbaum A, Gropman A, Wong LJ. Scaglia F, et al. Among authors: whiteman da. Genet Med. 2006 Oct;8(10):641-52. doi: 10.1097/01.gim.0000237781.10594.d1. Genet Med. 2006. PMID: 17079881 Free article.

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