Axelrod F - Search Results

1

Prenatal diagnostic testing for familial dysautonomia using linked genetic markers.

Oddoux C, Reich E, Axelrod F, Blumenfeld A, Maayan C, Slaugenhaupt S, Gusella J, Ostrer H. Oddoux C, et al. Among authors: axelrod f. Prenat Diagn. 1995 Sep;15(9):817-26. doi: 10.1002/pd.1970150905. Prenat Diagn. 1995. PMID: 8559751

2

Neoplasia in familial dysautonomia: a 20-year review in a young patient population.

Gold-von Simson G, Romanos-Sirakis E, Maayan C, Axelrod FB. Gold-von Simson G, et al. J Pediatr. 2009 Dec;155(6):934-6. doi: 10.1016/j.jpeds.2009.04.055. J Pediatr. 2009. PMID: 19914433

3

Survival in familial dysautonomia: Impact of early intervention.

Axelrod FB, Goldberg JD, Ye XY, Maayan C. Axelrod FB, et al. J Pediatr. 2002 Oct;141(4):518-23. doi: 10.1067/mpd.2002.127088. J Pediatr. 2002. PMID: 12378191

4

Identification of the first non-Jewish mutation in familial Dysautonomia.

Leyne M, Mull J, Gill SP, Cuajungco MP, Oddoux C, Blumenfeld A, Maayan C, Gusella JF, Axelrod FB, Slaugenhaupt SA. Leyne M, et al. Among authors: axelrod fb. Am J Med Genet A. 2003 May 1;118A(4):305-8. doi: 10.1002/ajmg.a.20052. Am J Med Genet A. 2003. PMID: 12687659

5

Growth hormone treatment in children with familial dysautonomia.

Kamboj MK, Axelrod FB, David R, Geffner ME, Novogroder M, Oberfield SE, Turco JH, Maayan C, Kohn B. Kamboj MK, et al. J Pediatr. 2004 Jan;144(1):63-7. doi: 10.1016/j.jpeds.2003.10.065. J Pediatr. 2004. PMID: 14722520

6

Gynecological aspects of female familial dysautonomia.

Maayan C, Sela O, Axelrod F, Kidron D, Hochner-Celnikier D. Maayan C, et al. Among authors: axelrod f. Isr Med Assoc J. 2000 Sep;2(9):679-83. Isr Med Assoc J. 2000. PMID: 11062768 Free article.

7

[Localization of the familial dysautonomia gene to chromosome 9q31-33 and the development of a genetic test for the disease].

Blumenfeld A, Axelrod FB, Tamper V, Maayan C. Blumenfeld A, et al. Among authors: axelrod fb. Harefuah. 1995 Jan 15;128(2):97-100. Harefuah. 1995. PMID: 7721187 Review. Hebrew. No abstract available.

8

Exclusion of familial dysautonomia from more than 60% of the genome.

Blumenfeld A, Axelrod FB, Trofatter JA, Maayan C, Lucente DE, Slaugenhaupt SA, Liebert CB, Ozelius LJ, Haines JL, Breakefield XO, et al. Blumenfeld A, et al. Among authors: axelrod fb. J Med Genet. 1993 Jan;30(1):47-52. doi: 10.1136/jmg.30.1.47. J Med Genet. 1993. PMID: 8093738 Free PMC article.

9

Localization of the gene for familial dysautonomia on chromosome 9 and definition of DNA markers for genetic diagnosis.

Blumenfeld A, Slaugenhaupt SA, Axelrod FB, Lucente DE, Maayan C, Liebert CB, Ozelius LJ, Trofatter JA, Haines JL, Breakefield XO, et al. Blumenfeld A, et al. Among authors: axelrod fb. Nat Genet. 1993 Jun;4(2):160-4. doi: 10.1038/ng0693-160. Nat Genet. 1993. PMID: 8102296

10

Prenatal diagnosis of familial dysautonomia by analysis of linked CA-repeat polymorphisms on chromosome 9q31-q33.

Eng CM, Slaugenhaupt SA, Blumenfeld A, Axelrod FB, Gusella JF, Desnick RJ. Eng CM, et al. Among authors: axelrod fb. Am J Med Genet. 1995 Nov 20;59(3):349-55. doi: 10.1002/ajmg.1320590314. Am J Med Genet. 1995. PMID: 8599360

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