Results 61 to 70 of about 8,023 (253)

Elephas jeffersoni ulna

, 1924
Ulna of E. jeffersoni. 5-9-22 B.

core   +1 more source

Left Ulna.

, 2012
Left Ulna in cranial (A), caudal (B), medial (C), lateral (D), proximal (E), distal (F).
George H. K. Sinapius (155398), David A. Elliott (102758), Scott A. Hocknull (155386), Trish Sloan (155393), Alex G. Cook (150321), Matt A. White (155381)   +5 more
core   +1 more source

The Homozygous p.(Arg215Ter) Variant in XRCC2 Is Associated With Atypical Fanconi Anemia Without Major Hematological Abnormalities in Childhood

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Fanconi Anemia (FA) is the most frequent inherited bone marrow failure syndrome. A role for the XRCC2 gene in FA was suspected in 2012 and confirmed in 2016, but only two affected individuals have been described thus far, and no long‐term follow‐up is available.
Sabina Cenciarelli, Giulia Bruna Marchetti, Maria Iascone, Maria Grazia Patricelli, Sara Giangiobbe, Gabriella Cinzia Pozzobon, Miriam Nella Savini, Fabio Giglio, Alessandro Aiuti, Paola Carrera, Francesca Ferrua, Angela Peron   +11 more
wiley   +1 more source

Treatment of a forelimb fracture and rehabilitation of a free-ranging Iberian Wolf (Canis lupus signatus)

Pesquisa Veterinária Brasileira, 2016
: The surgical treatment of an exposed compounded comminuted fracture of the right radius and ulna in a free-ranging adult female Iberian Wolf (Canis lupus signatus) with an osteosynthesis plate and screws and subsequent post-operative care are described.
Filipe C. Silva, Roberto F. Sargo, Luís C. Sousa, Helena Rio-Maior, Ricardo Brandão, Nuno Santos, Francisco Álvares, Isabel R. Dias   +7 more
doaj   +1 more source

Ulna VGL file

, 2016
Can be opened with vgsutiomax for reconstruction of the ...
Brandon Hedrick (3288471), Jason Schein (3288468), Jennifer Anné (499318)   +2 more
core   +1 more source

PUS7 Deficiency: Phenotypical Expansion of PUS7‐Related Neurodevelopmental Disorders

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Pathogenic variants in PUS7, encoding pseudouridine synthase 7, cause a rare neurodevelopmental disorder marked by intellectual disability, microcephaly, short stature, and behavioral disturbances. Since the first report in 2018, only 16 patients have been described.
Alice Muda, Barbara Belmessieri, Patrizia Accorsi, Jessica Galli, Edoardo Errichiello, Lucio Giordano   +5 more
wiley   +1 more source

Fracturedislocations of the proximal ulna

Acta Orthopaedica et Traumatologica Turcica, 2020
Abstract Objective: To investigate the relationship between injury patterns, complications, and the functional outcomes of patients with proximal-ulna fracture-dislocations. Methods: Retrospective analysis of 15 patients (10 men, 5 women; mean age, 49.1 years; mean follow-up 49 months) with 6 anterior and 9 posterior fracture-dislocations of the ...
Gereli, Arel, Nalbantoglu, Ufuk, Dikmen, Goksel, Seyhan, Mustafa, Turkmen, Metin   +4 more
openaire   +2 more sources

Right ulna and radius.

, 2015
Right ulna and radius.
Kyung-Seok Hu (816540), Jae Joon Hwang (655043), Eun Jin Woo (816539), Won-Joon Lee (591719)   +3 more
core   +1 more source

Spectrum of Congenital Anomalies in Myhre Syndrome—Insights Into Effects Brought by Altered TGF‐β Signaling via Gain‐of‐Function Variants in SMAD4

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome is a rare genetic disorder characterized by progressive multisystem involvement. Gain‐of‐function missense heterozygous variants affecting the Ile500 residue and Arg496 residue of the SMAD4 gene are implicated in this condition.
Kawmadi Gunawardena, Alessandro De Falco, Deborah Osio, Eleanor Sherlock, Emma Kivuva, Erina Sasaki, Francis H. Sansbury, Nayana Lahiri, Patricia Foley, Sahar Mansour, Shane McKee, Tazeen Ashraf, Nicola Brunetti‐Pierri, Usha Kini   +13 more
wiley   +1 more source

Congenital Radioulnar Synostosis Review: Recommendations and Treatment Outcomes

Children
Background/Objectives: Congenital radioulnar synostosis (CRS) is a rare congenital disorder of the elbow joint caused by the abnormal fusion of the radius and ulna during fetal development, leading to limited forearm rotation and functional impairment ...
Sergi Alabau-Rodriguez, Jose Felix Garrido Ferrer, Xavier Bulló Mir, Lidia Ana Martín Dominguez, Albert Pardo Pol, Francisco Soldado Carrera   +5 more
doaj   +1 more source