Hereditary Primitive Tetraploidy - Articles - Scientific Research Publishing

GJB2 Gene Related Nonsyndromic Hearing Loss in Mazandaran Province, North of Iran (Articles)

Elaheh Hosseini, Seyed Saeid Mousavi, Atefeh Khoshaein, Fatemeh Daneshpour, Moosa Rajabi Vandchali, S. Mohammad Bagher Hashemi-Soteh

Open Journal of Genetics Vol.10 No.3, September 30, 2020

DOI: 10.4236/ojgen.2020.103005 762 Downloads 2,672 Views Citations
Diabetes Mellitus Revealing a Rabson-Mendenhall Syndrome: A Case Report (Articles)

Samia Bentaleb, Siham Belmaati Cherkaoui, Sana Abourazzak, Mustapha Hida

Open Journal of Endocrine and Metabolic Diseases Vol.15 No.2, February 24, 2025

DOI: 10.4236/ojemd.2025.152003 137 Downloads 666 Views Citations
Chordomas and Their Consideration in the Radiographic Differential of Extra-Axial Lesions of the Central Nervous (Articles)

Shih-Shan Lang, Jayesh P. Thawani, Anousheh Sayah, Sriram Venneti, Danielle Brewington, Eric L. Zager, Stephen J. Dante

Open Journal of Modern Neurosurgery Vol.2 No.3, July 19, 2012

DOI: 10.4236/ojmn.2012.23012 4,978 Downloads 8,909 Views Citations
A case report on retroperitoneal PNET/EWS (Articles)

Zhanqiang Zhang, Honglan Yu, Yingying Shi, Hanping Shi

Case Reports in Clinical Medicine Vol.2 No.6, September 12, 2013

DOI: 10.4236/crcm.2013.26098 4,369 Downloads 7,148 Views Citations
Primitive Mammoth Hunters and the Earliest Breed of Dog (Articles)

Petr N. Kolosov

Natural Resources Vol.5 No.3, March 28, 2014

DOI: 10.4236/nr.2014.53011 5,299 Downloads 8,321 Views Citations
Primary Vulvar Ewing Sarcoma in a 30-Year-Old Woman: A Case Report (Case Report)

Fatoumata Matokoma Sidibe, Hajar Ouahbi, Rajae Kanab, Layla Tahiri, Fatim Zhara El Mrabet, Samia Arifi, Hind El Fatemi, Nawfel Mellas

Case Reports in Clinical Medicine Vol.7 No.3, March 21, 2018

DOI: 10.4236/crcm.2018.73022 1,204 Downloads 3,312 Views Citations
The Orbital Graph of Primitive Group with Socle A₇ × A₇ (Articles)

Jing Wu, Chang Wang, Jinlong Yang, Hong Xu

Advances in Pure Mathematics Vol.12 No.3, March 10, 2022

DOI: 10.4236/apm.2022.123012 256 Downloads 950 Views Citations
A Rare Case of Primitive Neuroectodermal Tumor of the Amygdala: A Case Report and Literature Review (Articles)

Niama Ghozali, Hajar Bakouri, Kamal Saiss, Yassine Sbaiti, Khadija Darif, Mounia Amzerin, Nabila Sella, Mohammed El Hfid, Fatima Zahra El M’Rabet

Open Access Library Journal Vol.11 No.6, June 28, 2024

DOI: 10.4236/oalib.1111736 60 Downloads 530 Views Citations
On the Hyperferritinemia and Hereditary Cataract Syndrome (Articles)

Maria José Perez-Lucena, María Sierra Moreno-Rosel, María Sagarra-Tió, Jordi Félez

Open Journal of Blood Diseases Vol.2 No.1, March 1, 2012

DOI: 10.4236/ojbd.2012.21002 4,778 Downloads 8,540 Views Citations
Perioperative anesthetic management in pediatric hereditary angioedema; case report (Articles)

M. Nuri Deniz, Aylin Incesu, Elvan Erhan, Gulden Ugur

Open Journal of Pediatrics Vol.2 No.4, December 13, 2012

DOI: 10.4236/ojped.2012.24050 4,197 Downloads 7,427 Views Citations
Course of Atypical Manifestations of a Case of Charcot-Marie-Tooth Disease over 35 Years of Clinical Observation (Articles)

Giuseppe Lanza, Luisa Vinciguerra, Valentina Puglisi, Daniela Modica, Alfio Catalano, Giuseppe Zelante, Riccardo Ricceri, Lorenzo Lupo, Salvatore Giuffrida, Manuela Pennisi

Neuroscience and Medicine Vol.4 No.3, September 10, 2013

DOI: 10.4236/nm.2013.43023 4,584 Downloads 6,984 Views Citations
Verification of the Validity of the NPT Treatment in Hereditary Spastic Paraplegia: An Investigation Performed by Application of Random Matrix Theory (Articles)

Elio Conte, Ken Ware, Riccardo Marvulli, Giancarlo Ianieri, Marisa Megna

World Journal of Neuroscience Vol.6 No.1, December 9, 2015

DOI: 10.4236/wjns.2016.61001 6,681 Downloads 8,218 Views Citations
Novel ACLV1 Mutation Identified in Late Onset Hereditary Hemorrhagic Telangiectasia (Articles)

Cory Patrick, Kaitlin McIntyre, Jeremy Ramidial, Sano Joa, Vijaykumar Dinsukhlal Zaveri, Damien Hansra

International Journal of Otolaryngology and Head & Neck Surgery Vol.5 No.4, July 18, 2016

DOI: 10.4236/ijohns.2016.54027 2,608 Downloads 5,022 Views Citations
Identifying Unique Protein Alterations Caused by SPTLC1 Mutations in a Transfected Neuronal Cell Model (Articles)

Scott E. Stimpson, Anu Shanu, Jens R. Coorssen, Simon J. Myers

World Journal of Neuroscience Vol.6 No.4, November 30, 2016

DOI: 10.4236/wjns.2016.64035 2,452 Downloads 4,103 Views Citations
This article belongs to the Special Issue on Neurodegeneration
Anesthetical Management of a Patient with Hereditary Muscle Sensory Neuropathy Type 2: Case of a 17-Year Old with Sacral Dermoid and a Short Overview of the Anesthesiological Considerations (Articles)

Martin Lasič, Ana Lasič, Caroline Oberleitner, Fugger Claudia, Ernst Trampitsch

Open Journal of Anesthesiology Vol.11 No.1, January 26, 2021

DOI: 10.4236/ojanes.2021.111003 622 Downloads 2,293 Views Citations
Hereditary Angioedema in Pregnancy and Management without Recombinant Human C1-INH (Articles)

Natália Paseto Pilati, Maria Alexandrina Zanatta, Daniele Camila Maltauro, Gabrielle Behenck, Edimárlei Gonsales Valério, Fernanda Oliveira Castilhos, Eduardo Vettorazzi-Stuczynski, Daniela Vanessa Vettori, Janete Vettorazzi

Open Journal of Obstetrics and Gynecology Vol.11 No.11, November 11, 2021

DOI: 10.4236/ojog.2021.1111137 321 Downloads 1,907 Views Citations
Hereditary Multiple Exostoses (HME) with Peroneal Nerve Compresion: A Case Report (Articles)

Onarisa Ayu, Muhammad Iqbal

International Journal of Medical Physics, Clinical Engineering and Radiation Oncology Vol.12 No.2, May 17, 2023

DOI: 10.4236/ijmpcero.2023.122006 273 Downloads 1,083 Views Citations
Hypothetical Willingness to Share the Genetic Test Results among the Relatives of Individuals with HBOC: A Study on the Japanese Population (Articles)

Ikumi Kataoka, Chieko Itaki, Tomisato Miura

Advances in Breast Cancer Research Vol.14 No.1, January 9, 2025

DOI: 10.4236/abcr.2025.141002 138 Downloads 694 Views Citations
Mitotic Slippage Process Concealed Cancer-Sought Chromosome Instability Mechanism (S-CIN) (Articles)

Kirsten H. Walen

Journal of Cancer Therapy Vol.8 No.6, June 30, 2017

DOI: 10.4236/jct.2017.86052 1,439 Downloads 2,702 Views Citations
Epigenetic Enabled Normal Human Cells, Lead to First Cell’s Unique Division System, Driving Tumorigenesis Evolution (Articles)

Kirsten H. Walen

Journal of Cancer Therapy Vol.13 No.1, January 25, 2022

DOI: 10.4236/jct.2022.131004 304 Downloads 1,202 Views Citations

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