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	1.	Autosomal recessive Oliver-McFarlane syndrome: retinitis pigmentosa, short stature (GH deficiency), trichomegaly, and hair anomalies or CPD syndrome (chorioretinopathy-pituitary dysfunction). [electronic resource] by Haimi, Motti Gershoni-Baruch, Ruth Producer: 20080227 In: American journal of medical genetics. Part A vol. 138A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Prevalence and significance of mutations in the familial Mediterranean fever gene in Henoch-Schönlein purpura. [electronic resource] by Gershoni-Baruch, Ruth Broza, Yiftah Brik, Riva Producer: 20040114 In: The Journal of pediatrics vol. 143 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Cisplatin treatment triggers familial Mediterranean fever attacks. [electronic resource] by Toubi, Elias Gershoni-Baruch, Ruth Kuten, Abraham Producer: 20030509 In: Tumori vol. 89 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Permanent neonatal diabetes. [electronic resource] by Bakri, Doua Gershoni-Baruch, Ruth Shehadeh, Naim Producer: 20040527 In: The Israel Medical Association journal : IMAJ vol. 6 Availability: No items available. Save to lists Add to cart (remove)
	5.	Socio-demographic and clinical profile of BRCA1/2 mutation carriers opting for prophylactic oophorectomy. [electronic resource] by Dagan, Efrat Gil, Sharon Gershoni-Baruch, Ruth Producer: 20080925 In: Preventive medicine vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Infantile familial Mediterranean fever. [electronic resource] by Brik, Riva Shinawi, Marwan Gershoni-Baruch, Ruth Producer: 20040123 In: The Israel Medical Association journal : IMAJ vol. 5 Availability: No items available. Save to lists Add to cart (remove)
	7.	Mutations in the glucocerebrosidase gene and Parkinson's disease in Ashkenazi Jews. [electronic resource] by Aharon-Peretz, Judith Rosenbaum, Hanna Gershoni-Baruch, Ruth Producer: 20041112 In: The New England journal of medicine vol. 351 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	The differential contribution of MEFV mutant alleles to the clinical profile of familial Mediterranean fever. [electronic resource] by Gershoni-Baruch, Ruth Brik, Riva Shinawi, Marwan Livneh, Avi Producer: 20020822 In: European journal of human genetics : EJHG vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Henoch-Schonlein purpura: polymorphisms in thrombophilia genes. [electronic resource] by Dagan, Efrat Brik, Riva Broza, Yiphtah Gershoni-Baruch, Ruth Producer: 20070222 In: Pediatric nephrology (Berlin, Germany) vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Aberration of 3q and monosomy 7 in a child with acute myelogenous leukemia. [electronic resource] by Haimi, Motti Elhasid, Ronit Moustafa, Nivin Gershoni-Baruch, Ruth Producer: 20070411 In: Cancer genetics and cytogenetics vol. 174 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Colchicine as a therapeutic option in periodic fever, aphthous stomatitis, pharyngitis, cervical adenitis (PFAPA) syndrome. [electronic resource] by Butbul Aviel, Yonatan Tatour, Sameh Gershoni Baruch, Ruth Brik, Riva Producer: 20161213 In: Seminars in arthritis and rheumatism vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Mutations in the glucocerebrosidase gene and Parkinson disease: phenotype-genotype correlation. [electronic resource] by Aharon-Peretz, Judith Badarny, Samih Rosenbaum, Hanna Gershoni-Baruch, Ruth Producer: 20060412 In: Neurology vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Tel Hashomer camptodactyly syndrome in identical twin infants. [electronic resource] by Smolkin, Tatiana Blazer, Shraga Gershoni-Baruch, Ruth Makhoul, Imad R Producer: 20120117 In: Clinical dysmorphology vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Pulmonary manifestations and function tests in children genetically diagnosed with FMF. [electronic resource] by Brik, Riva Gershoni-Baruch, Ruth Shinawi, Marwan Barak, Larissa Bentur, Lea Producer: 20031008 In: Pediatric pulmonology vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	"I do not want my baby to suffer as I did"; prenatal and preimplantation genetic diagnosis for BRCA1/2 mutations: a case report and genetic counseling considerations. [electronic resource] by Dagan, Efrat Gershoni-Baruch, Ruth Kurolap, Alina Goldberg, Yael Fried, Georgeta Producer: 20150330 In: Genetic testing and molecular biomarkers vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Familial Mediterranean fever: the segregation of four different mutations in 13 individuals from one inbred family: genotype-phenotype correlation and intrafamilial variability. [electronic resource] by Gershoni-Baruch, Ruth Shinawi, Marwan Shamaly, Hussein Katsinetz, Leah Brik, Riva Producer: 20020808 In: American journal of medical genetics vol. 109 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Mutations in CYP11B1 and congenital adrenal hyperplasia in Moroccan Jews. [electronic resource] by Paperna, Tamar Gershoni-Baruch, Ruth Badarneh, Kader Kasinetz, Leah Hochberg, Ze'ev Producer: 20051006 In: The Journal of clinical endocrinology and metabolism vol. 90 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Androgen receptor CAG repeat length in Jewish Israeli women who are BRCA1/2 mutation carriers: association with breast/ovarian cancer phenotype. [electronic resource] by Dagan, Efrat Friedman, Eitan Paperna, Tamar Carmi, Nirit Gershoni-Baruch, Ruth Producer: 20030610 In: European journal of human genetics : EJHG vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	MEFV, TNF1rA, CARD15 and NLRP3 mutation analysis in PFAPA. [electronic resource] by Dagan, Efrat Gershoni-Baruch, Ruth Khatib, Ihab Mori, Adi Brik, Riva Producer: 20100429 In: Rheumatology international vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Male sex coupled with articular manifestations cause a 4-fold increase in susceptibility to amyloidosis in patients with familial Mediterranean fever homozygous for the M694V-MEFV mutation. [electronic resource] by Gershoni-Baruch, Ruth Brik, Riva Lidar, Merav Shinawi, Marwan Livneh, Avi Producer: 20030512 In: The Journal of rheumatology vol. 30 Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 70 results.