Works matching DE "ECTRODACTYLY"

Results: 31

Split hand phenomenon: An early marker for amyotrophic lateral sclerosis.

Published in:

Revista Mexicana de Neurociencia, 2021, v. 22, n. 4, p. 141, doi. 10.24875/RMN.20000135

By:

Galnares-Olalde, Javier A.;
López-Hernández, Juan C.;
de Saráchaga-Adib, Jorge;
Cervantes-Uribe, Roberto;
Vargas-Cañas, Edwin S.

Publication type:

Article

Researching Malformations in Frogs of the Pelophylax esculentus Complex (Amphibia: Anura) in the Natural Populations of the Trakhtemyriv Peninsula (Ukraine).

Published in:

KnE Life Sciences, 2018, v. 2018, p. 117, doi. 10.18502/kls.v4i3.2112

By:

Nekrasova, O. D.;
Kuibida, V. V.

Publication type:

Article

LOBSTER CLAW SYNDROME (ECTRODACTYLY) IN A GERMAN SHEPHERD PUP.

Published in:

Journal of Indian Veterinary Association, 2023, v. 21, n. 1, p. 102, doi. 10.55296/JIVA/21.1.2023.102-104

By:

T., Giggin;
Jennes, Deny;
Ramankutty, Soumya;
Nair, Sudheesh S.;
S., Anoop;
K. D., John Martin

Publication type:

Article

Bhlha9 regulates apical ectodermal ridge formation during limb development.

Published in:

2018

By:

Kataoka, Kensuke;
Matsushima, Takahide;
Ito, Yoshiaki;
Sato, Tempei;
Yokoyama, Shigetoshi;
Asahara, Hiroshi

Publication type:

journal article

A child with type I ulnar ray deficiency.

Published in:

2018

By:

Gyu Hyeong Lee;
Ja Hea Gu

Publication type:

Case Study

Prenatal Diagnosis of Bilateral Ectrodactyly and Radial Agenesis Associated with Trisomy 10 Mosaicism.

Published in:

Case Reports in Genetics, 2013, p. 1, doi. 10.1155/2013/592702

By:

Lévy, Jonathan;
Jouannic, Jean-Marie;
Saada, Julien;
Dhombres, Ferdinand;
Siffroi, Jean-Pierre;
Portnoï, Marie-France

Publication type:

Article

SPLIT HAND SYNDROME AND THE SPLIT HAND INDEX IN ALS PATIENTS.

Published in:

Romanian Journal of Neurology, 2018, v. 17, n. 2, p. 57, doi. 10.37897/rjn.2018.2.1

By:

Antonescu, Florian;
Adam, Marin;
Popa, Constantin;
Tuta, Sorin

Publication type:

Article

Partial carpal arthrodesis for a case of ectrodactyly in a 10-month-old Samoyed.

Published in:

Australian Veterinary Practitioner, 2019, v. 49, n. 2, p. 36

By:

Tipler, A. E.;
Moses, P. A.

Publication type:

Article

Terminal latency abnormality in amyotrophic lateral sclerosis without split hand syndrome.

Published in:

2017

By:

Park, Donghwi;
Park, Jin-Sung

Publication type:

journal article

19q13.11 microdeletion: Clinical features overlapping ectrodactyly ectodermal dysplasia‐clefting syndrome phenotype.

Published in:

2018

By:

Abe, Kikue Terada;
Rizzo, Isabela M. P. O.;
Coelho, Ana L. V.;
Sakai, Jr, Nilo;
Carvalho, Daniel R.;
Speck‐Martins, Carlos E.

Publication type:

Case Study

Split-Hand Malformation in a 4-Year-Old Child.

Published in:

Case Reports in Pediatrics, 2017, p. 1, doi. 10.1155/2017/6073619

By:

Meshram, Girish Gulab;
Hura, Kanwaljeet Singh;
Kaur, Neeraj

Publication type:

Article

Poster 365: Proximal and Distal Patellar Realignment for Chronic Patellar Dislocation in Ectrodactyly and Congenital Type 2 Deficiency of the Tibia: A Case Report.

Published in:

2010

By:

Evans, Ake;
Ayyoub, Ziyad;
Ben‐Youssef, Ramzi;
Eberly, Vance;
Hsin, Ken;
Nallegowda, Mallikarjuna;
Richardson, Henry A.;
Tien, Phuong Q.

Publication type:

Abstract

Surgical management of ectrodactyly in a Turkish Kangal dog.

Published in:

Veterinary Journal of Ankara University / Ankara Universitesi Veteriner Fakultesi Dergisi, 2017, v. 64, n. 3, p. 229, doi. 10.1501/vetfak_0000002803

By:

YARDIMCI, Cenk;
ÖNYAY, Taylan;
İNAL, Kamil Serdar;
ÖZBAKIR, Birsen Deniz;
ÖZAK, Ahmet

Publication type:

Article

Síndrome de Karsch-Neugebauer: Reporte de caso.

Published in:

Ginecología y Obstetricia de México, 2023, v. 91, n. 10, p. 774, doi. 10.24245/gom.v91i10.8918

By:

Sandoval Quiñonez, Paul Alberto;
Naranjo González, María Luisa;
Lianes, Joel Murillo;
Favela Heredia, César Enrique;
Ordorica, Dalia Magaña;
Quintero, Paul González;
Ortiz, Fred Morgan;
Gámez Meza, Alán Hamid;
Castro Apodaca, Francisco Javier

Publication type:

Article

Congenital Malformations Resembling VACTERL Association in a Golden Retriever.

Published in:

Journal of the American Animal Hospital Association, 2018, v. 54, n. 1, p. 60, doi. 10.5326/JAAHA-MS-6236

By:

Gamito-Gómez, Araceli;
Gutierrez-Quintana, Rodrigo;
Wessmann, Annette

Publication type:

Article

Ectrodactyly-ectodermal dysplasia-clefting syndrome with unusual cutaneous vitiligoid and psoriasiform lesions due to a novel single point TP63 gene mutation.

Published in:

2019

By:

Wawrzycki, Bartłomiej;
Pietrzak, Aldona;
Chodorowska, Grażyna;
Filip, Agata A.;
Petit, Veronique;
Rudnicka, Lidia;
Dybiec, Ewa;
Rakowska, Adriana;
Sobczyńska-Tomaszewska, Agnieszka;
Kanitakis, Jean

Publication type:

Letter to the Editor

Nonsyndromic Split Hand/ Foot Malformation: Ectrodactyly.

Published in:

2016

By:

S., Ray;
P. C., Jain

Publication type:

Case Study

Surgical Ectrodactyly Repair Using Limb-lengthening and Bone Tissue Engineering Techniques in a Toy Dog Breed.

Published in:

In Vivo, 2020, v. 34, n. 2, p. 815, doi. 10.21873/invivo.11843

By:

MUN-IK LEE;
HO-HYUN KWAK;
JUN-HYUNG KIM;
HYEOK-SOO SHIN;
HEUNG-MYONG WOO;
BYUNG-JAE KANG

Publication type:

Article

Genetic regulatory pathways of split‐hand/foot malformation.

Published in:

Clinical Genetics, 2019, v. 95, n. 1, p. 132, doi. 10.1111/cge.13434

By:

Kantaputra, Piranit N.;
Carlson, Bruce M.

Publication type:

Article

<italic>WNT10B</italic> mutations associated with isolated dental anomalies.

Published in:

Clinical Genetics, 2018, v. 93, n. 5, p. 992, doi. 10.1111/cge.13218

By:

Kaewgahya, M.;
Intachai, W.;
German, R.;
Kantaputra, P. N.;
Hutsadaloi, A.;
Koparal, M.;
Leethanakul, C.;
Tolun, A.;
Ketudat Cairns, J. R.

Publication type:

Article

First direct evidence of involvement of a homozygous loss‐of‐function variant in the <italic>EPS15L1</italic> gene underlying split‐hand/split‐foot malformation.

Published in:

Clinical Genetics, 2018, v. 93, n. 3, p. 699, doi. 10.1111/cge.13152

By:

Umair, M.;
Ullah, A.;
Abbas, S.;
Ahmad, F.;
Basit, S.;
Ahmad, W.

Publication type:

Article

Goltz-Gorlin syndrome: a rare cause of ectrodactyly.

Published in:

2020

By:

Bhattacharjee, Rajsmita;
Tekumalla, Sindhuja;
De, Dipankar

Publication type:

journal article

First-Trimester Sonographic Evaluation of Palatine Clefts: A Novel Diagnostic Approach.

Published in:

Journal of Ultrasound in Medicine, 2017, v. 36, n. 7, p. 1397, doi. 10.7863/ultra.16.05084

By:

Lakshmy, Selvaraj Ravi;
Deepa, Selvaraj;
Rose, Nity;
Mookan, Senthilkumar;
Agnees, Joy

Publication type:

Article

Successful preterm pregnancy in a rare variation of Herlyn-Werner-Wunderlich syndrome: a case report.

Published in:

2018

By:

Cappello, Stefania;
Piccolo, Eleonora;
Cucinelli, Francesco;
Casadei, Luisa;
Piccione, Emilio;
Salerno, Maria Giovanna

Publication type:

journal article

Back to Basics.

Published in:

Journal of Forensic Identification, 2018, v. 68, n. 1, p. 160

By:

Siegel, Sandy

Publication type:

Article

A comprehensive functional classification of cleft hand: The DAST concept.

Published in:

Indian Journal of Plastic Surgery, 2017, v. 50, n. 3, p. 244, doi. 10.4103/ijps.IJPS_8_17

By:

Sharma, Alok;
Sharma, Namita

Publication type:

Article

Split hand index and ulnar to median ratio in Hirayama disease and amyotrophic lateral sclerosis.

Published in:

Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, 2017, v. 18, n. 7/8, p. 598, doi. 10.1080/21678421.2017.1336561

By:

Kalita, Jayantee;
Kumar, Surendra;
Misra, Usha K.;
Neyaz, Zafar

Publication type:

Article

Reverse split hand syndrome: Dissociated intrinsic hand muscle atrophy pattern in Hirayama disease/brachial monomelic amyotrophy.

Published in:

Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, 2017, v. 18, n. 1/2, p. 10, doi. 10.1080/21678421.2016.1223140

By:

Singh, Ravinder-Jeet;
Preethish-Kumar, Veeramani;
Polavarapu, Kiran;
Vengalil, Seena;
Prasad, Chandrajit;
Nalini, Atchayaram

Publication type:

Article

Split‑hand/feet malformation: A rare syndrome.

Published in:

2016

By:

Gane, Bahubali D.;
Natarajan, P.

Publication type:

Case Study

A novel description of a syndrome consisting of 7q21.3 deletion including DYNC1I1 with preserved DLX5/6 without ectrodactyly: a case report.

Published in:

2016

By:

Ramos-Zaldívar, Héctor M.;
Martínez-Irías, Daniel G.;
Espinoza-Moreno, Nelson A.;
Napky-Rajo, José S.;
Bueso-Aguilar, Tulio A.;
Reyes-Perdomo, Karla G.;
Montes-Gambarelli, Jimena A.;
Euceda, Isis M.;
Ponce-Barahona, Aldo F.;
Gámez-Fernández, Carlos A.;
Moncada-Arita, Wilberg A.;
Palomo-Bermúdez, Victoria A.;
Jiménez-Faraj, Julia E.;
Hernández-Padilla, Amanda G.;
Olivera, Denys A.;
Robertson, Kevin J.;
Leiva-Sanchez, Luis A.;
Herrera-Paz, Edwin Francisco

Publication type:

journal article

Holoprosencephaly in an Egyptian baby with ectrodactyly-ectodermal dysplasia-cleft syndrome: a case report.

Published in:

2012

By:

Metwalley Kalil, Kotb Abbass;
Fargalley, Hekma Saad

Publication type:

journal article