Lambert D - Search Results

1

Mutational spectrum of NSDHL in CHILD syndrome.

Bornholdt D, König A, Happle R, Leveleki L, Bittar M, Danarti R, Vahlquist A, Tilgen W, Reinhold U, Poiares Baptista A, Grosshans E, Vabres P, Niiyama S, Sasaoka K, Tanaka T, Meiss AL, Treadwell PA, Lambert D, Camacho F, Grzeschik KH. Bornholdt D, et al. Among authors: lambert d. J Med Genet. 2005 Feb;42(2):e17. doi: 10.1136/jmg.2004.024448. J Med Genet. 2005. PMID: 15689440 Free PMC article. No abstract available.

2

Clinical and genetic studies of Birt-Hogg-Dubé syndrome.

Khoo SK, Giraud S, Kahnoski K, Chen J, Motorna O, Nickolov R, Binet O, Lambert D, Friedel J, Lévy R, Ferlicot S, Wolkenstein P, Hammel P, Bergerheim U, Hedblad MA, Bradley M, Teh BT, Nordenskjöld M, Richard S. Khoo SK, et al. Among authors: lambert d. J Med Genet. 2002 Dec;39(12):906-12. doi: 10.1136/jmg.39.12.906. J Med Genet. 2002. PMID: 12471204 Free PMC article.

3

Keutel syndrome: further characterization and review.

Teebi AS, Lambert DM, Kaye GM, Al-Fifi S, Tewfik TL, Azouz EM. Teebi AS, et al. Among authors: lambert dm. Am J Med Genet. 1998 Jun 30;78(2):182-7. Am J Med Genet. 1998. PMID: 9674914 Review.

4

The Camera-Marugo-Cohen syndrome: report of two new patients.

Lambert DM, Watters G, Andermann F, Der Kaloustian VM. Lambert DM, et al. Am J Med Genet. 1999 Sep 17;86(3):208-14. doi: 10.1002/(sici)1096-8628(19990917)86:3<208::aid-ajmg3>3.0.co;2-h. Am J Med Genet. 1999. PMID: 10482867

5

Not Camera-Marugo-Cohen syndrome but diploid/triploid mixoploidy.

Lambert DM, Watters G, Andermann F, Der Kaloustian VM. Lambert DM, et al. Am J Med Genet. 2001 Dec 15;104(4):343-4. doi: 10.1002/ajmg.10074. Am J Med Genet. 2001. PMID: 11754073 No abstract available.

6

In vivo variability of TMA oxidation is partially mediated by polymorphisms of the FMO3 gene.

Lambert DM, Mamer OA, Akerman BR, Choinière L, Gaudet D, Hamet P, Treacy EP. Lambert DM, et al. Mol Genet Metab. 2001 Jul;73(3):224-9. doi: 10.1006/mgme.2001.3189. Mol Genet Metab. 2001. PMID: 11461189

7

Trimethylaminuria is caused by mutations of the FMO3 gene in a North American cohort.

Akerman BR, Lemass H, Chow LM, Lambert DM, Greenberg C, Bibeau C, Mamer OA, Treacy EP. Akerman BR, et al. Among authors: lambert dm. Mol Genet Metab. 1999 Sep;68(1):24-31. doi: 10.1006/mgme.1999.2885. Mol Genet Metab. 1999. PMID: 10479479

8

Evaluation of out-of-pocket pay genetic testing in a publicly funded healthcare system.

Grant P, Cook CB, Langlois S, Nuk J, Mung S, Zhang Q; GenCOUNSEL Study; Lynd LD, Austin J, Elliott AM. Grant P, et al. Clin Genet. 2023 Apr;103(4):424-433. doi: 10.1111/cge.14276. Epub 2023 Jan 5. Clin Genet. 2023. PMID: 36504324

9

Short-chain hydroxyacyl-coenzyme A dehydrogenase deficiency presenting as unexpected infant death: A family study.

Treacy EP, Lambert DM, Barnes R, Boriack RL, Vockley J, O'brien LK, Jones PM, Bennett MJ. Treacy EP, et al. Among authors: lambert dm. J Pediatr. 2000 Aug;137(2):257-9. doi: 10.1067/mpd.2000.107467. J Pediatr. 2000. PMID: 10931422

10

Fibroblasts from HPV-negative oropharynx squamous cell carcinomas stimulate the release of osteopontin from cancer cells via the release of IL-6.

Hendawi NY, Crane HL, Mehanna H, Bolt R, Lambert DW, Hunter KD. Hendawi NY, et al. Among authors: lambert dw. Front Oral Health. 2024 May 13;5:1390081. doi: 10.3389/froh.2024.1390081. eCollection 2024. Front Oral Health. 2024. PMID: 38803348 Free PMC article.

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