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Article Listing - Swiss Medical ForumSwiss Medical Forum
medicalforum.ch
Luisa Bonafé, Cecilia Giunta, Carol C Hasler, Marco Janner, Marius Kränzlin, Bianca Link, Christian Meier, Leonard E Ramseier, Marianne Rohrbach, ...
Découverte d’un Gène Responsable du Syndrome de Petite Taille Sévère...
www.myscience.ch
de gauche à droite : Andrea Superti-Furga, Dresse Luisa Bonafé, Dresse Sheila Unger. Le syndrome de « Kenny-Caffey » est une maladie rare ...
Turabian
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Ballhausen, Diana, Delphine Egli, Myriam Bickle-Graz, Nicoletta Bianchi, and Luisa Bonafé. “Born at 27 Weeks of Gestation With Classical PKU: Challenges of ... › get › t...
Born at 27 weeks of gestation with classical PKUpagepress.org
www.pagepress.org
— Nicoletta Bianchi Clinical Nutrition Unit, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland. Luisa Bonafé Division of Molecular ...
Interessen
A novel mutation in the sulfate transporter gene SLC26A2 (DTDST)...
jmg.bmj.com
Luisa Bonafé, MD, PhD. Division of Molecular Pediatrics. Centre Hospitalier Universitaire Vaudois. Clinique Infantile Av. P. Decker 2.
A novel mutation in the sulfate transporter gene SLC26A2 ...Journal of Medical Genetics
jmg.bmj.com
— Dr Luisa Bonafé, Division of Molecular Pediatrics, Centre Hospitalier Universitaire Vaudois, Clinique Infantile , Av. P. Decker 2, ...
Ausbildung
A novel form of ischio-vertebral syndromeScholars Portal Journals
journals.scholarsportal.info
... Sophia Hollander · Tanja Velten · Kerstin Reicherter · Jürgen Spranger · Stephen Robertson · Luisa Bonafé · Bernhard Zabel · Andrea Superti-Furga ...
Herkunft
Raphael Spada Rebechi e Renata Mendes Bonafégeneaminas.com.br
www.geneaminas.com.br
Árvore genealógica · Parentes próximos · Descendentes · Famílias às quais pertence. Tiveram 2 filhas. Laura Bonafé Rebechi · Luisa Bonafé Rebechi.
Bücher
Eight years experience from a skeletal dysplasia referral center in a...
biblio.ugent.be
... Fransiska Malfait UGent, Delfien Syx UGent, Raoul C Hennekam, Luisa Bonafe, Sheila Unger and Andrea Superti-Furga; organization.
Whole-exome sequencing detects somatic mutations of pub H-BRSpub.h-brs.de › authorsearch › author › Luisa+Bonafé › docId › start › rows
pub.h-brs.de
... Gen Nishimura, Sheila Unger, Jörn Oliver Sass, Joris A. Veltman, Han G. Brunner, Luisa Bonafé, Carlo Dionisi-Vici, Andrea Superti-Furga ...
Inherited Metabolic Diseases: A Clinical Approachgoogle.de
books.google.de
... Laboratory of Molecular Medicine, Bambino Gesu' Children's Research Hospital, Rome, Italy Luisa Bonafé Centre des Maladies Moléculaires (CMM), ...
Physician’s Guide to the Laboratory Diagnosis of Metabolic ...google.de
books.google.de
Disorders of Phenylalanine and Tetrahydrobiopterin Metabolism NENAD BLAU, LUISA BoNAFé, MILAN E. BLASKOVICS 1.1 Introduction Hyperphenylalaninemia, ...
Dokumente zum Namen
Diagnosis of Dopa-responsive Dystonia and Other ...Oxford Academic
academic.oup.com
von L Bonafé · · Zitiert von: 120 — Diagnosis of Dopa-responsive Dystonia and Other Tetrahydrobiopterin Disorders by the Study of Biopterin Metabolism in Fibroblasts. Luisa Bonafé,.
Glypican-6 promotes the growth of developing long bones ...Rockefeller University Press
rupress.org
von M Capurro · · Zitiert von: 49 — Luisa Bonafe,. Luisa Bonafe. 3. Center for Molecular Diseases, Lausanne University Hospital, Lausanne, Switzerland. Search for other works by this author on ...
EBSCOhost | | Early neurological impairment and severe...
web.a.ebscohost.com
Luisa Bonafé & Sarah Fattet & Jean-François Tolsa. Received: 6 November Revised: 29 April Accepted: 2 May Published online: 14 June ...
Lungenbeteiligung bei erwachsenen Patienten mit angeborenen ...Karger Publishers
karger.com
Luisa Bonafé. Luisa Bonafé. a Centre des Maladies Moléculaires, Service de Médecine Génétique, Lausanne, Suisse;. Search for other works by this author on:. von C Tran · — Luisa Bonafé. Luisa Bonafé. a Centre des Maladies Moléculaires, Service de Médecine Génétique, Lausanne, Suisse;.
Wissenschaftliche Veröffentlichungen
FreiDok plus - Bonafé, Luisa
freidok.uni-freiburg.de
Jahr, Titel, Rolle, Publikationstyp , Mutations in B3GALT6, which Encodes a Glycosaminoglycan Linker Region Enzyme, Cause a Spectrum of Skeletal and ...
Reviewer acknowledgement 2013Orphanet Journal of Rare Diseases
ojrd.biomedcentral.com
— Luisa Bonafé. Switzerland. Renato Borgatti. Italy. Salud Borrego. Spain. Dorin Bogdan Borza. United States of America. Patrice Bouvagnet.
Discovery – Mutated GPC6 Gene Key To Type Of Dwarfism | Science 2.0
www.science20.com
Scientists have discovered the gene behind Recessive Omodysplasia, a rare skeletal disease characterised by short-limbed dwarfism and craniofacial anomalies.
Gene identified, responsible for a spectrum of disorders affecting...
www.sciencedaily.com
Researchers have identified a gene that when mutated is responsible for a spectrum of disorders affecting the bones and connective tissue. This finding opens...
Veröffentlichungen allgemein
PDF file download - Skeldys.orgYUMPU
www.yumpu.com
— Luisa Bonafé, Lausanne. Pia Hermanns, Freiburg. Ekkehart Lausch, Mainz. Gerd Scherer, Freiburg.
European Journal of Pediatrics | Volume 168, issue 8Springer
link.springer.com
Marine Jequier Gygax; Eliane Roulet-Perez; Luisa Bonafé. Content type: Original Paper; Published: 13 November 2008; Pages:
Mutations in FKBP10 cause recessive osteogenesis BioMedSearch
www.biomedsearch.com
Brian P Kelley,1,2 Fransiska Malfait,3 Luisa Bonafe,4 Dustin Baldridge,1 Erica Homan,1 Sofie Symoens,3. Andy Willaert,3 Nursel Elcioglu,5 Lionel Van ...
Luisa Bonafé's Research on carbohydrate sulfotransferases (keratan...
www.curehunter.com
Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, ...
Video & Audio
maria luisa bonafé brisolaYouTube
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maria luisa bonafé brisola. @marialuisabonafebrisola4954No videos. More about this channel. Subscribe. HomePlaylistsChannels. maria luisa bonafé brisola. @marialuisabonafebrisola @marialuisabonafebrisola4954 No videos. More about this channel. Subscribe. Home. Playlists.
Artikel & Meinungen
Twitter-Nachrichten: Université de LausanneTwitter
Luisa Bonafé vient d'être nommée professeure associée à la Faculté de biologie et de médecine #métabolisme http://bit.ly/1d8fP0s.
Ausgabe Nr Swiss Medical Forum
medicalforum.ch
Luisa Bonafé, Cecilia Giunta, Carol C Hasler, Marco Janner, Marius Kränzlin, Bianca Link, Christian Meier, Leonard E Ramseier, Marianne Rohrbach, ... › detail › edn › smf
Sonstiges
MARIA LUISA BONAFE BRAGA - Credores Massa Falida da S. A....
ffx.com.br
O site de informções para os credores da massa falida das empresas S. A. Viação Aérea RioGrandense / Rio Sul / Nordeste.
Maria Luisa Bonafé Braga Motajusbrasil.com.br
www.jusbrasil.com.br
Pesquisar e Consultar sobre Maria Luisa Bonafé Braga Mota. Acesse o Jusbrasil e tenha acesso a Notícias, Artigos, Jurisprudência, Legislação, ...
Death of Madame Luisa BONAFE ( )Enaos
www.enaos.be
Death of Madame Luisa BONAFE ( ). enaos.net, a place where we can pay homage to those we have loved and respected.
Bonafe Namensbedeutung und -herkunftNames Encyclopedia
de.namespedia.com
Luisa Bonafe (1) Mateo Bonafe (1) Margarita Bonafe (1) Magdalena Bonafe (1) Marcelino Bonafe (1) Bernardo Bonafe (1) Bartomeu Bonafe (1) Virginie Bonafe (1)
Death of Madame Luisa BONAFE ( ) [en-GB], Deceased
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Décès de Madame Luisa BONAFE ( ) [fr-BE]. Défunte. enaos.net, un lieu où nous pouvons rendre hommage a ceux que nous avons ...
Décès de Madame Luisa BONAFE ( )foret-tejean.net
www.foret-tejean.net
— Décès de Madame Luisa BONAFE ( ). enaos.net, un lieu où nous pouvons rendre hommage a ceux que nous avons aimés et respectés.
Luisa BONAFE, veuve C. VRANCX de Flémalle - en mémoireen mémoire
enmemoire.sudinfo.be
— Luisa BONAFE, veuve C. VRANCX de Flémalle est décédée le 05 Septembre à l'âge de 75 ans. Toutes nos condoléances.
Death of Madame Luisa BONAFE ( )
www.enaos.be
· Décès de Madame Luisa BONAFE ( ) [fr-BE]. Défunte. enaos.net, un lieu où nous pouvons rendre hommage a ceux que nous avons aimés et ...
Pr Luisa BONAFÉ Clinical expert - Orphanet
www.orpha.net
CMM - Centre des Maladies Moléculaires; Service de médecine génétique; Centre Hospitalier Universitaire Vaudois CHUV - Hôpital Beaumont -; Avenue de ...
17. Basler Symposium für Kinderorthopädie - Wissenschaftliches...
www.kmb-lentzsch.de
Luisa Bonafé: : Diskussion: : Pause: Anatomische Besonderheiten Vorsitzende: C. Hasler / T. Wirth: : Becken und Hüfte Fritz Hefti: : Untere ...
Osteogenesis imperfecta: Klinik, Diagnose und Management vom Kindes-...
docplayer.org
Osteogenesis imperfecta: Klinik, Diagnose und Management vom Kindes- bis ins Erwachsenenalter Luisa Bonafé a, Cecillia Giunta b, Carol Hasler d, Marco Janner f ...
Le dépistage sélectif des maladies métaboliques au cabinet du...
docplayer.org
Le dépistage sélectif des maladies métaboliques au cabinet du pédiatre Luisa Bonafé, Diana Ballhausen, Division de Pédiatrie Moléculaire, CHUV, Lausanne Les ...
Skelettdysplasien mit Mutationen im Sulfat Transporter Gen das...
docplayer.org
Skelettdysplasien mit Mutationen im Sulfat Transporter Gen das -Spektrum Andreas Zankl, Luisa Bonafé, Andrea Superti-Furga Division de Pédiatrie Moléculaire ...
Luisa BonafeRevue Médicale Suisse
www.revmed.ch
Luisa Bonafe. Centre des maladies moléculaires. Département médico-chirurgical de pédiatrie. CHUV, Lausanne. Articles. 4 mai
A faithful JAGGED1 haploinsufficiency mouse model OA.mg
oa.mg
... Stanley F. Nelson, Luisa Bonafé, Andrea Superti-Furga, Shiro Ikegawa, Deborah Krakow, Daniel H. Cohn, Tom Kirchhausen, Matthew L. Warman, David R. Beier. › work › hep
4. März 2017, Lausanne :: Allianz Seltener KrankheitenProRaris
www.proraris.com
Präsentation Luisa Bonafé und Bérengère Aubry-Rozier, CHUV (FR) · Präsentation Therese Stutz Steiger, SVOI · Präsentation Loredana D'Amato Sizonenko und ...
Atelosteogenesis - Medical
lpamrs.memberclicks.net
Source/Author: Luisa Bonafé, MD, PhD, Lauréane Mittaz-Crettol, PhD, Diana Ballhausen, MD, and Andrea Superti-Furga, MD - GeneReviews. Web-based ...
Bonafé, J.L.: د Z-Library مفت الکترونیکی کتابتون
ps.art1lib.org
Alberto B. Burlina, Luisa Bonafé, Franco Zacchello. مجله: Seminars in Perinatology. کال: ژبه: english. فایل: PDF, MB. ستاسی تیګی: ... › ...
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