Ben Pode-Shakked

ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 12

Top Venues

American journal of medical genetics. Part A

Annals of internal medicine

Journal of medical genetics

Nutrients

This page only lists publications with an associated author ORCID identifier.

Publications

Emily Stenke, Cara Dunne, Anthea Bryce-Smyth, Michelle Hurley, Ben Pode-Shakked, Yair Anikster, Tricia Mei-Mei Tan, Anna M Kowalka, Paul Bech, Billy Bourke
Reversal of Intestinal Failure With Teduglutide in PERCC1 -Associated Enteropathy: A Case Report. Annals of internal medicine (2024)
Emily Stenke, Cara Dunne, Anthea Bryce-Smyth, Michelle Hurley, Ben Pode-Shakked, Yair Anikster, Tricia Mei-Mei Tan, Anna M Kowalka, Paul Bech, Billy Bourke
Reversal of Intestinal Failure With Teduglutide in PERCC1 -Associated Enteropathy: A Case Report. Annals of internal medicine 177 (8) (2024)
Jean-Madeleine de Sainte Agathe, Ben Pode-Shakked, Sophie Naudion, Vincent Michaud, Benoit Arveiler, Patricia Fergelot, Jean Delmas, Boris Keren, Céline Poirsier, Fowzan Sami Alkuraya, Brahim Tabarki, Eric Bend, Kellie Davis, E Martina Bebin, Michelle L Thompson, Emily M Bryant, Matias Wagner, Iris Hannibal, Jerica Lenberg, Martin Krenn, Kristen M Wigby, Jennifer R Friedman, Maria Iascone, Anna Cereda, Térence Miao, Eric Le Guern, Emanuela Argilli, Elliott Sherr, Oana Caluseriu, Timothy Tidwell, Pinar Bayrak-Toydemir, Caroline Hagedorn, Melanie Brugger, Katharina Vill, Francois-Dominique Morneau-Jacob, Wendy K Chung, Kathryn Nicole Weaver, Joshua W Owens, Ammar Husami, Bimal P Chaudhari, Brandon S Stone, Katie Burns, Rachel Li, Iris M de Lange, Margaux Biehler, Emmanuelle Ginglinger, Bénédicte Gérard, Rolf W Stottmann, Aurélien Trimouille
ARF1 -related disorder: phenotypic and molecular spectrum. Journal of medical genetics (2023)
Ben Pode-Shakked, Yishay Ben-Moshe, Ortal Barel, Lilach C Regev, Maayan Kagan, Aviva Eliyahu, Dina Marek-Yagel, Danit Atias-Varon, Einat Lahav, Naomi Issler, Omer Shlomovitz, Rotem Semo Oz, Nitzan Kol, Nofar Mor, Ifat Bar-Joseph, Yulia Khavkin, Elisheva Javasky, Pazit Beckerman, Meidad Greenberg, Oded Volovelsky, Yael Borovitz, Miriam Davidovits, Orly Haskin, Hadas Alfandary, Shely Levi, Maital Kaidar, Ze'ev Katzir, Avital Angel-Korman, Rachel Becker-Cohen, Efrat Ben-Shalom, Adi Leiba, Eytan Mor, Amit Dagan, Itai M Pessach, Danny Lotan, Moshe Shashar, Yair Anikster, Annick Raas-Rothschild, Gideon Rechavi, Benjamin Dekel, Asaf Vivante
A multidisciplinary nephrogenetic referral clinic for children and adults-diagnostic achievements and insights. Pediatric nephrology (Berlin, Germany) 37 (7) (2022)
Shani Karklinsky, Shir Kugler, Omer Bar-Yosef, Andreea Nissenkorn, Anat Grossman-Jonish, Irit Tirosh, Asaf Vivante, Ben Pode-Shakked
Hereditary neuropathy with liability to pressure palsies (HNPP): Intrafamilial phenotypic variability and early childhood refusal to walk as the presenting symptom. Italian journal of pediatrics 48 (1) (2022)
Yoav Bolkier, Ortal Barel, Dina Marek-Yagel, Danit Atias-Varon, Maayan Kagan, Amir Vardi, David Mishali, Uriel Katz, Yishay Salem, Tal Tirosh-Wagner, Jeffrey M Jacobson, Annick Raas-Rothschild, Odelia Chorin, Aviva Eliyahu, Yarden Sarouf, Omer Shlomovitz, Alvit Veber, Nechama Shalva, Elisheva Javasky, Yishay Ben Moshe, Orna Staretz-Chacham, Gideon Rechavi, Shrikant Mane, Yair Anikster, Asaf Vivante, Ben Pode-Shakked
Whole-exome sequencing reveals a monogenic cause in 56% of individuals with laterality disorders and associated congenital heart defects. Journal of medical genetics (2021)
Dina Marek-Yagel, Aviva Eliyahu, Alvit Veber, Nechama Shalva, Amit Mary Philosoph, Ortal Barel, Elisheva Javasky, Ben Pode-Shakked, Neta Loewenthal, Yair Anikster, Orna Staretz-Chacham
Deep intronic variant in the ARSB gene as the genetic cause for Maroteaux-Lamy syndrome (MPS VI). American journal of medical genetics. Part A 185 (12) (2021)
Orna Staretz-Chacham, Ben Pode-Shakked, Eyal Kristal, Smadar Yaala Abraham, Keren Porper, Ohad Wormser, Ilan Shelef, Yair Anikster
The Effects of a Ketogenic Diet on Patients with Dihydrolipoamide Dehydrogenase Deficiency. Nutrients 13 (10) (2021)
Dina Marek-Yagel, Yoav Bolkier, Ortal Barel, Amir Vardi, David Mishali, Uriel Katz, Yishay Salem, Shachar Abudi, Omri Nayshool, Nitzan Kol, Annick Raas-Rothschild, Gideon Rechavi, Yair Anikster, Ben Pode-Shakked
A founder truncating variant in GDF1 causes autosomal-recessive right isomerism and associated congenital heart defects in multiplex Arab kindreds. American journal of medical genetics. Part A 182 (5) (2020)
Ben Pode-Shakked, Asaf Vivante, Ortal Barel, Shai Padeh, Dina Marek-Yagel, Alvit Veber, Shachar Abudi, Aviva Eliyahu, Irit Tirosh, Shiri Shpilman, Shirlee Shril, Friedhelm Hildebrandt, Mordechai Shohat, Yair Anikster
Progressive Pseudorheumatoid Dysplasia resolved by whole exome sequencing: a novel mutation in WISP3 and review of the literature. BMC medical genetics 20 (1) (2019)
Naomi Pode Shakked, Ortal Barel, Ben Pode-Shakked, Aviva Eliyahu, Amihood Singer, Omri Nayshool, Nitzan Kol, Annick Raas-Rothschild, Elon Pras, Mordechai Shohat
BRPF1-associated intellectual disability, ptosis, and facial dysmorphism in a multiplex family. Molecular genetics & genomic medicine 7 (6) (2019)
Michal Berkenstadt, Ben Pode-Shakked, Ortal Barel, Hila Barash, Reuven Achiron, Yinon Gilboa, Dvora Kidron, Annick Raas-Rothschild
LMOD3-Associated Nemaline Myopathy: Prenatal Ultrasonographic, Pathologic, and Molecular Findings. Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine 37 (7) (2018)

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Publication Activity (10 Years)

Top Topics

Top Venues

Ben Pode-Shakked