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Neue Form der seltenen Glasknochenkrankheit entdeckt - Innovations...
www.innovations-report.de
... Benno Röthlisberger, Marianne Rohrbach, Ingo Kennerknecht, David Eyre, Kanya Suphapeetiporn, Cecilia Giunta, Joan Marini, and Vorasuk ...
A Yale connection to Thailand—and the King of Siam | Yale School of...
medicine.yale.edu
When Kanya Suphapeetiporn, M. D.
NEUIGKEITEN AUS DER STIFTUNGSARBEIT. newsletter. Awards. Awareness....
docplayer.org
5 5 ALLIANCE KONFERENZ AM CHIEMSEE: FORSCHUNG FÜR SELTENE ERKRANKUNGEN UND PERSONALISIERTE MEDIZIN Mitglieder des neuen Netzwerkes (v.l.n.r.): Raz Somech (Tel Aviv), Josef Penninger (Wien), Kanya Suphapeetiporn (Bangkok), Scott Snapper (Boston), Christoph Klein (München), Ekrem ...
Netzwerk-Profile
LinkedIn: Kanya Suphapeetiporn | LinkedIn
ดูโพรไฟล์มืออาชีพของ Kanya Suphapeetiporn บน LinkedIn LinkedIn เป็นเครือข่ายธุรกิจที่ใหญ่ที่สุดให้โลก ที่ช่วยให้มืออาชีพเช่น Kanya Suphapeetiporn ...
Loop | Kanya Suphapeetiporn
loop.frontiersin.org
Kanya Suphapeetiporn. Professor. Chulalongkorn University. Bangkok, Thailand. View All. mini profile avatar Kanya Suphapeetiporn. Overview ...
Interessen
Absent expression of the osteoblast-specific maternally imprinted...
jmg.bmj.com
…spondence to Dr Kanya Suphapeetiporn, Division of Medical Genetics and Metabolism, Department of Pediatrics, Sor Kor Building 11th floor, King ...
Firmen-Mitarbeiter
Base - ten-for-rare: research on rare diseases and personalized...
www.ten-for-rare.com
Faculty of Medicine, Chulalongkorn University, Bangkok: Dr. Kanya Suphapeetiporn, Head of Medical Genetics and Metabolism Unit, Department of Pediatrics.
Bücher
Massive parallel sequencing as a new diagnostic approach for...
doaj.org
Information about the open-access article 'Massive parallel sequencing as a new diagnostic approach for phenylketonuria and tetrahydrobiopterin-deficiency in...
Texto completo (pdf) - Dialnet
dialnet.unirioja.es
Woraman Waidab, Kanya Suphapeetiporn, Chalurm- pon Srichom…. Association of cytokine-related gene expression with dengue infection severity. Pe-.
Molecular Vision: Articles by the Authors
www.molvis.org
Articles by Surasawadee Ausavarat · Articles by Chalurmpon Srichom… · Articles by Vilavun Puangsricharern · Articles by Kanya Suphapeetiporn.
Socio-economics of Personalized Medicine in Asia - Shirley Sun -...
books.google.de
The second decade of the twenty-first century has witnessed a surging interest in personalized medicine with the concomitant promise to enable more precise...
Musik
Full text of "Yale medicine : alumni bulletin of the School of...
archive.org
Joining Lanza in a discussion of the issues were Yale clinicians and ... been working on¬ site at Yale since January to inventory the contents of all the ... A Yale connection to Thailand—and the King of Siam When Kanya Suphapeetiporn, ...
Dokumente zum Namen
CONTENTS Page Speakers Programs Abstracts Acknowledgement Index - PDF...
healthdocbox.com
... Nikhil Thapar (U.K.) S-7-2 Management of Intractable Constipation …it Osatakul (Thailand) ... A reduced protein supply, more similar to the intake with breastfeeding, ... Following the demonstration that short-chain fatty …s stimulate colonic ... Kanya Suphapeetiporn 3, Vorasuk Shotelersuk 4, Santi Punnahitananda 5, ...
A novel PCCB mutation in a Thai patient with propionic …emia...
www.scienceopen.com
Authors: Thantrira Porntaveetus, Chalurmpon Srichom…,, Kanya Suphapeetiporn,,, Vorasuk Shotelersuk,. Publication date ( Electronic ):
Disorders with similar clinical phenotypes reveal underlying genetic...
www.deepdyve.com
Two syndromic cognitive impairment disorders have very similar craniofacial dysmorphisms. One is caused by mutations of SATB2 , a transcription regulator and...
Meta-analysis of two Chinese populations identifies an autoimmune...
www.scienceopen.com
The 95% concentration band is shown in grey, and the y = x line is shown in red. (0.13 MB TIF) Click Kanya Suphapeetiporn: . Vorasuk ...
Wissenschaftliche Veröffentlichungen
New type of rare brittle-bone disease discovered -- ScienceDaily
www.sciencedaily.com
Researchers have discovered the first X-chromosome-inherited type of the congenital disease osteogenesis imperfecta, also known as brittle-bone disease. The...
The most 5′ truncating homozygous mutation of WNT1 in ...bmcmedgenet.biomedcentral.com › ...
bmcmedgenet.biomedcentral.com
Chalurmpon Srichom…, Apiruk Sangsin, Kanya Suphapeetiporn & Vorasuk Shotelersuk. Excellence Center for Medical Genetics, the Thai ...
Veröffentlichungen allgemein
Kanya Suphapeetiporn | PubFactswww.pubfacts.com › author › Kanya+Suphapeetiporn
www.pubfacts.com
Eur J Med Genet Sep 11;63(9): Epub Jun 11. Center of Excellence for Medical Genomics, Medical Genomics C…er, Department of ...
Missing: Wunsiedel" | Must include: Wunsiedel"
Age-Related Reference Intervals for Blood Amino …s in Thai...
www.hindawi.com
Jaraspong Uaariyapanichkul, Sirinuch Chomtho, Kanya Suphapeetiporn, et al., “Age-Related Reference Intervals for Blood Amino …s in ...
Hyperostosis, Infantile Cortical | SpringerLinklink.springer.com › ...
link.springer.com
Kanya Suphapeetiporn; Vorasuk Shotelersuk. Kanya Suphapeetiporn. 1. Vorasuk Shotelersuk Division of Medical Genetics and Metabolism, Department of ...
Artikel & Meinungen
A novel PCCB mutation in a Thai patient with propionic …emia...
www.nature.com
Thantrira Porntaveetus ,; Chalurmpon Srichom… ,; Kanya Suphapeetiporn &; Vorasuk Shotelersuk. Human Genome Variation volume 2, ...
Sonstiges
"Mutations in Kinesin family member 6 reveal specific role in...
digitalcommons.wustl.edu
By Mia J. Konjikusic, Patra Yeetong, Curtis W. Boswell, et al., Published on
Generation and characterization of HLA-universal platelets derived...
pubmed.ncbi.nlm.nih.gov
Platelet demand has increased around the world. However, the inadequacy of donors, the risk of transfusion-transmitted infections and associated reactions, and...
Wiskott-Aldrich syndrome iPS cells produce megakaryocytes with...
pubmed.ncbi.nlm.nih.gov
PubMed comprises more than 30 million citations for biomedical literature from MEDLINE, life science journals, and online books. Citations may include links to...
Scilit | Article - Risk factors for autism spectrum disorder in the...
www.scilit.net
Scilit is a centralized platform for all published research literature, articles with a DOI or in PubMed are indexed within hours
Whole Genome and Exome Sequencing of Monozygotic Twins with Trisomy...
figshare.com
Whole Genome and Exome Sequencing of Monozygotic Twins with Trisomy 21, Discordant for a Congenital Heart Defect and Epilepsy
2nd MBE (Matrix Biology Europe) Conference Athens-Greece ...docplayer.net › ...
docplayer.net
Heparin chains contains several domains with specific sulfation patters that ... Ingo Kennerknecht 12, David R. Eyre 8, Kanya Suphapeetiporn 3,4, Cecilia Mosaiques Diagnostics GMBH, Hannover, Germany 4 University of ... short supply of donor islets and their poor survival and efficacy in the portal ...
ASTMH 57th Annual Meeting. Volume 79 December Number 6. Final...
docplayer.net
... Richard Paul 4, Paul Brey 5, Juliet E. Bryant 5 National Center for Laboratory ... infection severity Woraman Waidab, Kanya Suphapeetiporn, Usa Thisyakorn ...
Cell Biology Tree - Kanya Suphapeetiporn Family Tree
academictree.org
Cell Biology Tree: academic genealogy for researcher
Content Posted in | Health Sciences Research Commons |...
hsrc.himmelfarb.gwu.edu
Active and Passive Stress Management Mechanisms in Physically Active Young …s, ... Development of a Healthy and Sustainable Food Availability Inventory ... Chonchaiya, Kanya Suphapeetiporn, Apiwat Mutirangura, Tewin Tencomnao, ...
"Integrated genome-wide Alu methylation and transcriptome profiling...
hsrc.himmelfarb.gwu.edu
Kanya Suphapeetiporn · Apiwat Mutirangura · Tewin Tencomnao · Valerie W Hu, George Washington University · Tewarit Sarachana ...
21 Grand Casino Play
UBC-Point Grey The University of British Columbia 21 has a candidacy of found by Alfred M. Nicholas Spinelli( been) with Kanya Suphapeetiporn of Thailand, ...
Papers with the keyword Pycnodysostosis (Page 4) | Read by QxMD
read.qxmd.com
... an imbalance between the growing brain, its vascular supply and intraventricular ... Wipa Panmontha, Siraprapa Tongkobpetch, Kanya Suphapeetiporn, Vorasuk ... Polymerase chain reaction sequencing of the entire coding regions of CTSK ... with novel gene mutation and severe obstructive sleep apnoea: management ...
Phatchara Norbnop - ten-for-rare: research on rare diseases and...
www.ten-for-rare.com
... of Medicine, Chulalongkorn University, Thailand under mentoring of Professor Vorasuk Shotelersuk, MD and Professor Kanya Suphapeetiporn, MD, PhD.
Altmetric – Meta-analysis of two Chinese populations identifies an...
www.altmetric.com
... Xiang-Pei Li, Yingyos Avihingsanon, Pornpimol Rianthavorn, Thavatchai Deekajorndej, Kanya Suphapeetiporn, Vorasuk Shotelersuk, Shirley King Yee Ying, ...
A novel de novo COL1A1 mutation in a Thai boy with osteogenesis...
www.scielo.br
Kanya Suphapeetiporn. Vorasuk Shotelersuk. 1Inter-Department Program of Biomedical Sciences, Faculty of Graduate School, Chulalongkorn University, Bangkok, Thailand. 2Center of Excellence for Medical Genetics, Department of Pediatrics, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
Under the auspices of H.E. the President of the Hellenic Republic,...
docplayer.net
112) Researcher, Data Collection and Management, Centre for International ... Kanya Suphapeetiporn, Chalurmpon Srichom…, Siraprapa Tongkobpetch, ... OF THE PEDIATRIC QUALITY OF LIFE INVENTORY (PEDSQLTM) 4.0 … ...
University of Groningen. Dengue and Chikungunya virus van...
healthdocbox.com
010;6: e Welsch S, Miller S, Romero-Brey I, Merz A, Bleck CK, Walther P, et al Olarn Prommalikit 1, Woraman Waidab 2, Kanya Suphapeetiporn 3 and Usa ...
Molecular Vision: A novel p.E276K IDUA mutation...
www.molvis.org
…spondence to: Kanya Suphapeetiporn, M.D., Ph.D., Head of Division of Medical Genetics and Metabolism, Department of Pediatrics, Sor ...
Verwandte Suchanfragen zu Kanya Suphapeetiporn
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