Citations (35)
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Uner Tan & Meliha Tan. (2009) Unertan Syndrome: A New Variant of Unertan Syndrome: Running on All Fours in Two Upright-Walking Children. International Journal of Neuroscience 119:7, pages 909-918.
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Üner Tan. (2008) A Special Case of Anencephaly in an Early-Born Baby with an Exagerated Prognastic Face: Further Example for Human Devolution. International Journal of Neuroscience 118:6, pages 751-760.
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ÜNER TAN, SIBEL KARACA, MELIHA TAN, BEKIR YILMAZ, NAMIK KEMAL BAGCI, AYHAN OZKUR & SADRETTIN PENCE. (2008) UNERTAN SYNDROME: A CASE SERIES DEMONSTRATING HUMAN DEVOLUTION. International Journal of Neuroscience 118:1, pages 1-25.
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UNER TAN. (2008) UNERTAN SYNDROME: REVIEW AND REPORT OF FOUR NEW CASES. International Journal of Neuroscience 118:2, pages 211-225.
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Üner Tan, Sadrettin Pençe, Mustafa Yilmaz, Ayhan Özkur, Si˙bel Karaca, Meli˙ha Tan & Mehmet Karataş. (2008) “Unertan Syndrome” in two Turkish Families in Relation to Devolution and Emergence of Homo Erectus: Neurological Examination, MRI, and pet Scans. International Journal of Neuroscience 118:3, pages 313-336.
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ÜNER TAN. (2007) A WRIST-WALKER EXHIBITING NO “UNER TAN SYDNROME”: A THEORY FOR POSSIBLE MECHANISMS OF HUMAN DEVOLUTION TOWARD THE ATAVISTIC WALKING PATTERNS. International Journal of Neuroscience 117:1, pages 147-156.
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GILBERTO DE LIMA GARCIAS & MARIA DA GRAÇA MARTINO ROTH. (2007) A BRAZILIAN FAMILY WITH QUADRUPEDAL GAIT, SEVERE MENTAL RETARDATION, COARSE FACIAL CHARACTERISTICS, AND HIRSUTISM. International Journal of Neuroscience 117:7, pages 927-933.
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UNER TAN. (2006) EVIDENCE FOR “UNER TAN SYNDROME” AS A HUMAN MODEL FOR REVERSE EVOLUTION. International Journal of Neuroscience 116:12, pages 1539-1547.
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UNER TAN. (2006) EVIDENCE FOR “UNERTAN SYNDROME” AND THE EVOLUTION OF THE HUMAN MIND. International Journal of Neuroscience 116:7, pages 763-774.
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Articles from other publishers (26)
Rauan Kaiyrzhanov, Juan Darío Ortigoza‐Escobar, Brett W. Stringer, Manizha Ganieva, Vykuntaraju K. Gowda, Varunvenkat M. Srinivasan, Alfons Macaya, Andreas Laner, Enas Onbool, Randa Al‐Shammari, Mohammed Al‐Owain, Nicolas Deconinck, Catheline Vilain, Pauline Dontaine, Eleanor Self, Rabia Akram, Ghulam Hussain, Shahid Mahmood Baig, Javed Iqbal, Vincenzo Salpietro, Maedeh Neshatdoust, Mahboubeh Kasiri, Gozde Yesil, Turkan Uygur, Karen Pysden, Ian R. Berry, Cesar Augusto Alves, Jean Giacomotto, Henry Houlden & Reza Maroofian. (2024)
Clinical and Molecular Spectrum of Autosomal Recessive
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Gurusidheshwar M Wali & Gautam Wali. (2024) Quadrupedal locomotion in Uner Tan syndrome: A neurological viewpoint. Annals of Movement Disorders.
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Luíza Alves Corazza, Vinícius Lopes Braga, Thiago Yoshinaga Tonholo Silva, Flávio Moura Rezende Filho, Juliana Maria Ferraz Sallum, Orlando Graziani Povoas Barsottini & José Luiz Pedroso. (2023)
ATP8A2
‐Related Disorder: Beyond Cerebellar Ataxia
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Anastasia P. Grigorenko, Maria S. Protasova, Alexandra A. Lisenkova, Denis A. Reshetov, Tatiana V. Andreeva, Gilberto De Lima Garcias, Maria Da Graça Martino Roth, Andreas Papassotiropoulos & Evgeny I. Rogaev. (2022) Neurodevelopmental Syndrome with Intellectual Disability, Speech Impairment, and Quadrupedia Is Associated with Glutamate Receptor Delta 2 Gene Defect. Cells 11:3, pages 400.
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Malihe Mohamadian, Pegah Ghandil, Mohsen Naseri, Afsane Bahrami & Ali Akbar Momen. (2020) A novel homozygous variant in an Iranian pedigree with cerebellar ataxia, mental retardation, and dysequilibrium syndrome type 4. Journal of Clinical Laboratory Analysis 34:11.
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Claire Guissart, Alexander N. Harrison, Mehdi Benkirane, Ibrahim Oncel, Elif Acar Arslan, Anna K . Chassevent, Kristin Baraῆano, Lise Larrieu, Maria Iascone, Romano Tenconi, Mireille Claustres, Nesibe Eroglu-Ertugrul, Patrick Calvas, Haluk Topaloglu, Robert S. Molday & Michel Koenig. (2019) ATP8A2-related disorders as recessive cerebellar ataxia. Journal of Neurology 267:1, pages 203-213.
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Whitney G. Cole, Beatrix Vereijken, Jesse W. Young, Scott R. Robinson & Karen E. Adolph. (2018) Use it or lose it? Effects of age, experience, and disuse on crawling. Developmental Psychobiology 61:1, pages 29-42.
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Mara Cavallin, Maria A Rujano, Nathalie Bednarek, Daniel Medina-Cano, Antoinette Bernabe Gelot, Severine Drunat, Camille Maillard, Meriem Garfa-Traore, Christine Bole, Patrick Nitschké, Claire Beneteau, Thomas Besnard, Benjamin Cogné, Marion Eveillard, Alice Kuster, Karine Poirier, Alain Verloes, Jelena Martinovic, Laurent Bidat, Marlene Rio, Stanislas Lyonnet, M Louise Reilly, Nathalie Boddaert, Melanie Jenneson-Liver, Jacques Motte, Martine Doco-Fenzy, Jamel Chelly, Tania Attie-Bitach, Matias Simons, Vincent Cantagrel, Sandrine Passemard, Alexandre Baffet, Sophie Thomas & Nadia Bahi-Buisson. (2017) WDR81 mutations cause extreme microcephaly and impair mitotic progression in human fibroblasts and Drosophila neural stem cells. Brain 140:10, pages 2597-2609.
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Alain Frigon. (2017) The neural control of interlimb coordination during mammalian locomotion. Journal of Neurophysiology 117:6, pages 2224-2241.
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Gurusidheshwar Wali. (2016) Two Indian Families with Quadrupedal Locomotion Resembling Uner Tan Syndrome: A Video Document. Movement Disorders Clinical Practice 4:1, pages 49-50.
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Elisa Giorgio, Andrea Ciolfi, Elisa Biamino, Viviana Caputo, Eleonora Di Gregorio, Elga Fabia Belligni, Alessandro Calcia, Elena Gaidolfi, Alessandro Bruselles, Cecilia Mancini, Simona Cavalieri, Cristina Molinatto, Margherita Cirillo Silengo, Giovanni Battista Ferrero, Marco Tartaglia & Alfredo Brusco. (2016) Whole exome sequencing is necessary to clarify ID/DD cases with de novo copy number variants of uncertain significance: Two proof‐of‐concept examples. American Journal of Medical Genetics Part A 170:7, pages 1772-1779.
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Fusun Doldur-Balli, Mehmet Neset Ozel, Suleyman Gulsuner, Ayse B. Tekinay, Tayfun Ozcelik, Ozlen Konu & Michelle M. Adams. (2015) Characterization of a novel zebrafish (Danio rerio) gene, wdr81, associated with cerebellar ataxia, mental retardation and dysequilibrium syndrome (CAMRQ). BMC Neuroscience 16:1.
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John G. Morris & Padraic J. Grattan-SmithJohn G. Morris & Padraic J. Grattan-Smith. 2015. Manual of Neurological Signs. Manual of Neurological Signs.
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Liza J. Shapiro, Whitney G. Cole, Jesse W. Young, David A. Raichlen, Scott R. Robinson & Karen E. Adolph. (2014) Human Quadrupeds, Primate Quadrupedalism, and Uner Tan Syndrome. PLoS ONE 9:7, pages e101758.
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Pierre A. Guertin. (2014) Preclinical evidence supporting the clinical development of central pattern generator-modulating therapies for chronic spinal cord-injured patients. Frontiers in Human Neuroscience 8.
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Maria Traka, Kathleen J. Millen, Devon Collins, Benayahu Elbaz, Grahame J. Kidd, Christopher M. Gomez & Brian Popko. (2013) WDR81 Is Necessary for Purkinje and Photoreceptor Cell Survival. The Journal of Neuroscience 33:16, pages 6834-6844.
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Fatma Mujgan Sonmez, Joseph G. Gleeson, Figen Celep & Sibel Kul. (2012) The Very Low Density Lipoprotein Receptor–Associated Pontocerebellar Hypoplasia and Dysmorphic Features in Three Turkish Patients. Journal of Child Neurology 28:3, pages 379-383.
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Onur Emre Onat, Suleyman Gulsuner, Kaya Bilguvar, Ayse Nazli Basak, Haluk Topaloglu, Meliha Tan, Uner Tan, Murat Gunel & Tayfun Ozcelik. (2012) Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion. European Journal of Human Genetics 21:3, pages 281-285.
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Suleyman Gulsuner, Ayse Begum Tekinay, Katja Doerschner, Huseyin Boyaci, Kaya Bilguvar, Hilal Unal, Aslihan Ors, O. Emre Onat, Ergin Atalar, A. Nazli Basak, Haluk Topaloglu, Tulay Kansu, Meliha Tan, Uner Tan, Murat Gunel & Tayfun Ozcelik. (2011) Homozygosity mapping and targeted genomic sequencing reveal the gene responsible for cerebellar hypoplasia and quadrupedal locomotion in a consanguineous kindred. Genome Research 21:12, pages 1995-2003.
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Luis E. Kolb, Zulfikar Arlier, Cengiz Yalcinkaya, Ali K. Ozturk, Jennifer A. Moliterno, Ozdem Erturk, Fatih Bayrakli, Baris Korkmaz, Michael L. DiLuna, Katsuhito Yasuno, Kaya Bilguvar, Tayfun Ozcelik, Beyhan Tuysuz, Matthew W. State & Murat Gunel. (2010) Novel VLDLR microdeletion identified in two Turkish siblings with pachygyria and pontocerebellar atrophy. neurogenetics 11:3, pages 319-325.
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Şevket Akpınar. (2009) In restless legs syndrome, the neural substrates of the sensorimotor symptoms are also normally involved in upright standing posture and biped walking. Medical Hypotheses 73:2, pages 169-176.
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Tayfun OzcelikNurten AkarsuElif Uz, Safak Caglayan, Suleyman Gulsuner, Onur Emre Onat, Meliha Tan & Uner Tan. (2008)
Mutations in the very low-density lipoprotein receptor
VLDLR
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Niccolo Leo Caldararo. (2017) The Concepts of 'Species' and 'Population' in Considering Ancient DNA and Building Phylogenetic Trees of Hominid Evolution. SSRN Electronic Journal.
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