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Neurology
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May 24, 2006
Expanding the clinical spectrum of POMT1 phenotype
A D'Amico, A Tessa, C Bruno, et al.
The Journal of Pediatrics
|
June 4, 1999
Infantile encephalopathy associated with the MELAS A3243G mutation
C M Sue, C Bruno, A L Andreu, et al.
Immunologic Research
|
September 4, 2012
Influence of human immune cells on cancer: studies at the University of Colorado
Tullia C Bruno, Jena D French, Kimberly R Jordan, et al.
Neuromuscular Disorders : NMD
|
February 5, 2003
Autosomal dominant external ophthalmoplegia and bipolar affective disorder associated with a mutation in the ANT1 gene
G Siciliano, A Tessa, S Petrini, et al.
Oncogene
|
April 15, 2005
A 5'-distal enhanceosome in the PDGF-A gene is activated in choriocarcinoma cells via ligand-independent binding of vitamin D receptor and constitutive jun kinase signaling
Nancy G Pedigo, Hongxing Zhang, Maria E C Bruno, et al.
Human Reproduction (Oxford, England)
|
May 12, 2016
Survey of 243 ART patients having made a final disposition decision about their surplus cryopreserved embryos: the crucial role of symbolic embryo representation
C Bruno, C Dudkiewicz-Sibony, I Berthaut, et al.
Journal of Endocrinological Investigation
|
July 22, 2023
Combined evaluation of prolactin-induced peptide (PIP) and extracellular signal-regulated kinase (ERK) as new sperm biomarkers of FSH treatment efficacy in normogonadotropic idiopathic infertile men
F Mancini, F Di Nicuolo, E Teveroni, et al.
European Review for Medical and Pharmacological Sciences
|
February 12, 2021
Evaluation of Kisspeptin levels in prepubertal obese and overweight children: sexual dimorphism and modulation of antioxidant levels
A Mancini, D Currò, C Cipolla, et al.
The New England Journal of Medicine
|
September 30, 1999
Exercise intolerance due to mutations in the cytochrome b gene of mitochondrial DNA
A L Andreu, M G Hanna, H Reichmann, et al.
Neuropediatrics
|
October 12, 2005
Phenotypic heterogeneity in two unrelated Danon patients associated with the same LAMP-2 gene mutation
E Bertini, M A Donati, P Broda, et al.
Page
of 36
Search research articles
Search
Showing results (231-240 of 355) with videos related to
Sort By:
Page
of 36
Neurology
|
May 24, 2006
Expanding the clinical spectrum of POMT1 phenotype
A D'Amico, A Tessa, C Bruno, et al.
The Journal of Pediatrics
|
June 4, 1999
Infantile encephalopathy associated with the MELAS A3243G mutation
C M Sue, C Bruno, A L Andreu, et al.
Immunologic Research
|
September 4, 2012
Influence of human immune cells on cancer: studies at the University of Colorado
Tullia C Bruno, Jena D French, Kimberly R Jordan, et al.
Neuromuscular Disorders : NMD
|
February 5, 2003
Autosomal dominant external ophthalmoplegia and bipolar affective disorder associated with a mutation in the ANT1 gene
G Siciliano, A Tessa, S Petrini, et al.
Oncogene
|
April 15, 2005
A 5'-distal enhanceosome in the PDGF-A gene is activated in choriocarcinoma cells via ligand-independent binding of vitamin D receptor and constitutive jun kinase signaling
Nancy G Pedigo, Hongxing Zhang, Maria E C Bruno, et al.
Human Reproduction (Oxford, England)
|
May 12, 2016
Survey of 243 ART patients having made a final disposition decision about their surplus cryopreserved embryos: the crucial role of symbolic embryo representation
C Bruno, C Dudkiewicz-Sibony, I Berthaut, et al.
Journal of Endocrinological Investigation
|
July 22, 2023
Combined evaluation of prolactin-induced peptide (PIP) and extracellular signal-regulated kinase (ERK) as new sperm biomarkers of FSH treatment efficacy in normogonadotropic idiopathic infertile men
F Mancini, F Di Nicuolo, E Teveroni, et al.
European Review for Medical and Pharmacological Sciences
|
February 12, 2021
Evaluation of Kisspeptin levels in prepubertal obese and overweight children: sexual dimorphism and modulation of antioxidant levels
A Mancini, D Currò, C Cipolla, et al.
The New England Journal of Medicine
|
September 30, 1999
Exercise intolerance due to mutations in the cytochrome b gene of mitochondrial DNA
A L Andreu, M G Hanna, H Reichmann, et al.
Neuropediatrics
|
October 12, 2005
Phenotypic heterogeneity in two unrelated Danon patients associated with the same LAMP-2 gene mutation
E Bertini, M A Donati, P Broda, et al.
Page
of 36