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Danny Petronius

Research Profile

Physiology

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Publications

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Eli Sprecher; Margarita Indelman; Ziad Khamaysi; J Lugassy; Danny Petronius; Reuven Bergman
Galli-Galli disease is an acantholytic variant of Dowling-Degos disease.
Mordechai Mizrachi-Koren; Saar Shemer; Michal Morgan; Margarita Indelman; Ziad Khamaysi; Danny Petronius; Ora Bitterman-Deutsch; Hans Christian Hennies; Reuven Bergman; Eli Sprecher
Homozygosity mapping as a screening tool for the molecular diagnosis of hereditary skin diseases in consanguineous populations.
Orit Topaz; Daniel L Shurman; Reuven Bergman; Margarita Indelman; Paulina Ratajczak; Mordechai Mizrachi; Ziad Khamaysi; Doron M Behar; Danny Petronius; Vered Friedman; Israel Zelikovic; Sharon Raimer; Aryeh Metzker; Gabriele Richard; Eli Sprecher
Mutations in GALNT3, encoding a protein involved in O-linked glycosylation, cause familial tumoral calcinosis.

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All Publications

2007: Eli Sprecher; Margarita Indelman; Ziad Khamaysi; J Lugassy; Danny Petronius; Reuven Bergman
Galli-Galli disease is an acantholytic variant of Dowling-Degos disease.
The British journal of dermatology 2007;156(3):572-4.
2006: Mordechai Mizrachi-Koren; Saar Shemer; Michal Morgan; Margarita Indelman; Ziad Khamaysi; Danny Petronius; Ora Bitterman-Deutsch; Hans Christian Hennies; Reuven Bergman; Eli Sprecher
Homozygosity mapping as a screening tool for the molecular diagnosis of hereditary skin diseases in consanguineous populations.
Journal of the American Academy of Dermatology 2006;55(3):393-401.
2004: Orit Topaz; Daniel L Shurman; Reuven Bergman; Margarita Indelman; Paulina Ratajczak; Mordechai Mizrachi; Ziad Khamaysi; Doron M Behar; Danny Petronius; Vered Friedman; Israel Zelikovic; Sharon Raimer; Aryeh Metzker; Gabriele Richard; Eli Sprecher
Mutations in GALNT3, encoding a protein involved in O-linked glycosylation, cause familial tumoral calcinosis.
Nature genetics 2004;36(6):579-81.
2003: Danny Petronius; Reuven Bergman; Ofer Ben-Izhak; Ronit Leiba; Eli Sprecher
A comparative study of immunohistochemistry and electron microscopy used in the diagnosis of epidermolysis bullosa.
The American Journal of dermatopathology 2003;25(3):198-203.
2003: Dan Ciubotaru; Reuven Bergman; David Baty; Margarita Indelman; Ellen Pfendner; Danny Petronius; Hannah Moualem; Moien Kanaan; Dan Ben-Amitai; W H Irwin McLean; Jouni Uitto; Eli Sprecher
Epidermolysis bullosa simplex in Israel: clinical and genetic features.
Archives of dermatology 2003;139(4):498-505.
2002: Margarita Indelman; Reuven Bergman; raziel lurie; Gabriele Richard; Benjamin Miller; Danny Petronius; Dan Ciubutaro; Rina Leibu; Eli Sprecher
A missense mutation in CDH3, encoding P-cadherin, causes hypotrichosis with juvenile macular dystrophy.
The Journal of investigative dermatology 2002;119(5):1210-3.
2002: Danny Petronius; Reuven Bergman
Bullous pemphigoid in two young infants.
Pediatric dermatology 2002;19(2):119-21.
2001: Eli Sprecher; Reuven Bergman; Gabriele Richard; raziel lurie; Stavit A Shalev; Danny Petronius; Adel Shalata; Y Anbinder; Rina Leibu; Ido Perlman; Nadine Cohen; Raymonde Szargel
Hypotrichosis with juvenile macular dystrophy is caused by a mutation in CDH3, encoding P-cadherin.
Nature genetics 2001;29(2):134-6.