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Clinical Nutrition (Edinburgh, Scotland)
|
May 18, 2005
Effect of oral administration of a whole formula diet on nutritional and cognitive status in patients with Alzheimer's disease
Jordi Salas-Salvadó, Míriam Torres, Mercè Planas, et al.
Journal of Cutaneous Pathology
|
February 23, 2023
Essential thrombocythemia manifesting as livedoid and purpuric skin lesions: Report of two cases and literature review
Alejandro Lapeña Casado, Carlos Santonja, Mar García-García, et al.
International Journal of Obesity (2005)
|
December 13, 2018
Prefronto-cerebellar neuromodulation affects appetite in obesity
Elena M Marron, Raquel Viejo-Sobera, Guillem Cuatrecasas, et al.
American Journal of Medical Genetics. Part A
|
August 6, 2003
Turner phenotype in a girl with a 45,X/46,XX/47,XX,+18 mosaicism
Isabel Lorda-Sanchez, Maria Jose Trujillo, Pilar Gomez-Garre, et al.
American Journal of Medical Genetics. Part A
|
October 18, 2008
A small and active ring X chromosome in a female with features of Kabuki syndrome
L Rodríguez, D Diego-Alvarez, I Lorda-Sanchez, et al.
Veterinary Journal (London, England : 1997)
|
April 13, 2011
Chondroitin sulfate proteoglycan-4: a biomarker and a potential immunotherapeutic target for canine malignant melanoma
Saray Lorda Mayayo, Simone Prestigio, Lorella Maniscalco, et al.
Medicina Intensiva
|
May 17, 2011
[EICS (Extended Intensive Care Service): looking outside the ICU]
M S Holanda Peña, M J Domínguez Artiga, E Ots Ruiz, et al.
Clinical and Experimental Dermatology
|
March 13, 2021
Azathioprine hypersensitivity syndrome: report of two cases with cutaneous manifestations
C Moya-Martínez, L Núñez-Hipólito, S Barrio-González, et al.
Prenatal Diagnosis
|
March 4, 2000
Rapid identification of a small dicentric supernumerary marker derived from chromosome 16 with a modified FISH technique on amniotic fluid
R Sanz, M A Anabitarte, M E Querejeta, et al.
Molecular Vision
|
February 6, 2007
Partial paternal uniparental disomy (UPD) of chromosome 1 in a patient with Stargardt disease
R Riveiro-Alvarez, D Valverde, I Lorda-Sanchez, et al.
Page
of 25
Search research articles
Search
Showing results (161-170 of 242) with videos related to
Sort By:
Page
of 25
Clinical Nutrition (Edinburgh, Scotland)
|
May 18, 2005
Effect of oral administration of a whole formula diet on nutritional and cognitive status in patients with Alzheimer's disease
Jordi Salas-Salvadó, Míriam Torres, Mercè Planas, et al.
Journal of Cutaneous Pathology
|
February 23, 2023
Essential thrombocythemia manifesting as livedoid and purpuric skin lesions: Report of two cases and literature review
Alejandro Lapeña Casado, Carlos Santonja, Mar García-García, et al.
International Journal of Obesity (2005)
|
December 13, 2018
Prefronto-cerebellar neuromodulation affects appetite in obesity
Elena M Marron, Raquel Viejo-Sobera, Guillem Cuatrecasas, et al.
American Journal of Medical Genetics. Part A
|
August 6, 2003
Turner phenotype in a girl with a 45,X/46,XX/47,XX,+18 mosaicism
Isabel Lorda-Sanchez, Maria Jose Trujillo, Pilar Gomez-Garre, et al.
American Journal of Medical Genetics. Part A
|
October 18, 2008
A small and active ring X chromosome in a female with features of Kabuki syndrome
L Rodríguez, D Diego-Alvarez, I Lorda-Sanchez, et al.
Veterinary Journal (London, England : 1997)
|
April 13, 2011
Chondroitin sulfate proteoglycan-4: a biomarker and a potential immunotherapeutic target for canine malignant melanoma
Saray Lorda Mayayo, Simone Prestigio, Lorella Maniscalco, et al.
Medicina Intensiva
|
May 17, 2011
[EICS (Extended Intensive Care Service): looking outside the ICU]
M S Holanda Peña, M J Domínguez Artiga, E Ots Ruiz, et al.
Clinical and Experimental Dermatology
|
March 13, 2021
Azathioprine hypersensitivity syndrome: report of two cases with cutaneous manifestations
C Moya-Martínez, L Núñez-Hipólito, S Barrio-González, et al.
Prenatal Diagnosis
|
March 4, 2000
Rapid identification of a small dicentric supernumerary marker derived from chromosome 16 with a modified FISH technique on amniotic fluid
R Sanz, M A Anabitarte, M E Querejeta, et al.
Molecular Vision
|
February 6, 2007
Partial paternal uniparental disomy (UPD) of chromosome 1 in a patient with Stargardt disease
R Riveiro-Alvarez, D Valverde, I Lorda-Sanchez, et al.
Page
of 25