Rachmel A[au] - Search Results

Year	Number of Results
1981	2
1982	2
1983	2
1985	1
1986	2
1987	3
1988	2
1989	4
1990	3
1991	2
1992	3
1993	2
1995	1
1996	1
1997	2
1999	2
2000	1
2001	3
2002	1
2003	4
2004	1
2006	1
2009	1
2010	1
2022	0

1

[Biliglobulin].

Danon YL, Nitzan M, Rachmel A. Danon YL, et al. Among authors: rachmel a. Harefuah. 1982 Jan 1;102(1):37-8. Harefuah. 1982. PMID: 7095618 Hebrew. No abstract available.

2

Type 2 Gaucher disease occurs in Ashkenazi Jews but is surprisingly rare.

Aviner S, Garty BZ, Rachmel A, Baris HN, Sidransky E, Shuffer A, Attias J, Yaniv Y, Cohen IJ. Aviner S, et al. Among authors: rachmel a. Blood Cells Mol Dis. 2009 Nov-Dec;43(3):294-7. doi: 10.1016/j.bcmd.2009.08.004. Epub 2009 Sep 5. Blood Cells Mol Dis. 2009. PMID: 19734074 Free PMC article. Review.

3

Fructose-1,6-diphosphatase deficiency in Israel.

Moses SW, Bashan N, Flasterstein BF, Rachmel A, Gutman A. Moses SW, et al. Among authors: rachmel a. Isr J Med Sci. 1991 Jan;27(1):1-4. Isr J Med Sci. 1991. PMID: 1995492

4

Mass at the splenic hilum: a clue to torsion of a wandering spleen located in a normal left upper quadrant position.

Kessler A, Miller E, Keidar S, Blachar A, Sira LB, Weinberg M, Rachmel A. Kessler A, et al. Among authors: rachmel a. J Ultrasound Med. 2003 May;22(5):527-30. doi: 10.7863/jum.2003.22.5.527. J Ultrasound Med. 2003. PMID: 12751865

5

A randomized, double-blind study examining the comparative efficacies and safety of inhaled epinephrine and nasal decongestant in hospitalized infants with acute bronchiolitis.

Livni G, Rachmel A, Marom D, Yaari A, Tirosh N, Ashkenazi S. Livni G, et al. Among authors: rachmel a. Pediatr Infect Dis J. 2010 Jan;29(1):71-3. doi: 10.1097/INF.0b013e3181b0602e. Pediatr Infect Dis J. 2010. PMID: 19907355 Clinical Trial.

6

Alagille syndrome associated with moyamoya disease.

Rachmel A, Zeharia A, Neuman-Levin M, Weitz R, Shamir R, Dinari G. Rachmel A, et al. Am J Med Genet. 1989 May;33(1):89-91. doi: 10.1002/ajmg.1320330112. Am J Med Genet. 1989. PMID: 2750789

7

Periventricular brain heterotopias in a child with adrenocortical insufficiency, achalasia, alacrima, and neurologic abnormalities (Allgrove syndrome).

Zeharia A, Shuper A, Mimouni M, Kornreich L, Rachmel A, Lerman-Sagie T. Zeharia A, et al. Among authors: rachmel a. J Child Neurol. 1999 May;14(5):331-4. doi: 10.1177/088307389901400512. J Child Neurol. 1999. PMID: 10342602

8

Identification of a common mutation (Gly194Cys) in both Arab Moslem and Ashkenazi Jewish patients with dihydrolipoamide dehydrogenase (E3) deficiency: possible beneficial effect of vitamin therapy.

Hong YS, Korman SH, Lee J, Ghoshal P, Wu Q, Barash V, Kang S, Oh S, Kwon M, Gutman A, Rachmel A, Patel MS. Hong YS, et al. Among authors: rachmel a. J Inherit Metab Dis. 2003;26(8):816-8. doi: 10.1023/b:boli.0000010004.12053.5b. J Inherit Metab Dis. 2003. PMID: 14765544

9

Branhamella catarrhalis as a cause of suppurative arthritis.

Izraeli S, Flasterstein B, Shamir R, Rachmel A, Nitzan M, Drucker M, Samra Z. Izraeli S, et al. Among authors: rachmel a. Pediatr Infect Dis J. 1989 Apr;8(4):256-7. Pediatr Infect Dis J. 1989. PMID: 2497437 No abstract available.

10

Direct measurement of TP/GFR: a simple and reliable parameter of renal phosphate handling.

Stark H, Eisenstein B, Tieder M, Rachmel A, Alpert G. Stark H, et al. Among authors: rachmel a. Nephron. 1986;44(2):125-8. doi: 10.1159/000184216. Nephron. 1986. PMID: 3774075

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