Search research articles
Contact Us
Filters
Showing results (71-80 of 90) with videos related to
Page
of 9
Sort By:
The American Journal of Surgical Pathology
|
June 8, 2001
Cystic endocrine tumors of the pancreas: clinical, radiologic, and histopathologic features in 13 cases
B Ligneau, C Lombard-Bohas, C Partensky, et al.
Blood
|
June 15, 1992
Expression of the APO-1 antigen in Burkitt lymphoma cell lines correlates with a shift towards a lymphoblastoid phenotype
M H Falk, B C Trauth, K M Debatin, et al.
Annals of Surgery
|
July 22, 1998
Thymic carcinoids in multiple endocrine neoplasia type 1
B T Teh, J Zedenius, S Kytölä, et al.
Annales De Chirurgie
|
May 15, 2004
[Gastrinomas in multiple endocrine neoplasia type-1. A 127-case cohort study from the endocrine tumor group (ETG)]
P Goudet, F Peschaud, M Mignon, et al.
Endocrine-Related Cancer
|
October 26, 2013
Altered MENIN expression disrupts the MAFA differentiation pathway in insulinoma
Z Hamze, C Vercherat, A Bernigaud-Lacheretz, et al.
International Journal of Cancer
|
August 5, 2000
Malignant melanoma in patients with multiple endocrine neoplasia type 1 and involvement of the MEN1 gene in sporadic melanoma
B Nord, A Platz, K Smoczynski, et al.
Genomics
|
November 1, 1996
Definition of the minimal MEN1 candidate area based on a 5-Mb integrated map of proximal 11q13. The European Consortium on Men1, (GENEM 1; Groupe d'Etude des Néoplasies Endocriniennes Multiples de type 1)
A Courseaux, J Grosgeorge, P Gaudray, et al.
Human Genetics
|
September 1, 1997
Mapping of the gene encoding the B56 beta subunit of protein phosphatase 2A (PPP2R5B) to a 0.5-Mb region of chromosome 11q13 and its exclusion as a candidate gene for multiple endocrine neoplasia type 1 (MEN1)
S A Forbes, A A Pannett, J H Bassett, et al.
Journal of Medical Genetics
|
February 27, 2004
Germline and de novo mutations in the HRPT2 tumour suppressor gene in familial isolated hyperparathyroidism (FIHP)
A Villablanca, A Calender, L Forsberg, et al.
Clinical Genetics
|
July 4, 2015
Whole-exome sequencing improves the diagnosis yield in sporadic infantile spasm syndrome
S Dimassi, A Labalme, D Ville, et al.
Page
of 9
Search research articles
Search
Showing results (71-80 of 90) with videos related to
Sort By:
Page
of 9
The American Journal of Surgical Pathology
|
June 8, 2001
Cystic endocrine tumors of the pancreas: clinical, radiologic, and histopathologic features in 13 cases
B Ligneau, C Lombard-Bohas, C Partensky, et al.
Blood
|
June 15, 1992
Expression of the APO-1 antigen in Burkitt lymphoma cell lines correlates with a shift towards a lymphoblastoid phenotype
M H Falk, B C Trauth, K M Debatin, et al.
Annals of Surgery
|
July 22, 1998
Thymic carcinoids in multiple endocrine neoplasia type 1
B T Teh, J Zedenius, S Kytölä, et al.
Annales De Chirurgie
|
May 15, 2004
[Gastrinomas in multiple endocrine neoplasia type-1. A 127-case cohort study from the endocrine tumor group (ETG)]
P Goudet, F Peschaud, M Mignon, et al.
Endocrine-Related Cancer
|
October 26, 2013
Altered MENIN expression disrupts the MAFA differentiation pathway in insulinoma
Z Hamze, C Vercherat, A Bernigaud-Lacheretz, et al.
International Journal of Cancer
|
August 5, 2000
Malignant melanoma in patients with multiple endocrine neoplasia type 1 and involvement of the MEN1 gene in sporadic melanoma
B Nord, A Platz, K Smoczynski, et al.
Genomics
|
November 1, 1996
Definition of the minimal MEN1 candidate area based on a 5-Mb integrated map of proximal 11q13. The European Consortium on Men1, (GENEM 1; Groupe d'Etude des Néoplasies Endocriniennes Multiples de type 1)
A Courseaux, J Grosgeorge, P Gaudray, et al.
Human Genetics
|
September 1, 1997
Mapping of the gene encoding the B56 beta subunit of protein phosphatase 2A (PPP2R5B) to a 0.5-Mb region of chromosome 11q13 and its exclusion as a candidate gene for multiple endocrine neoplasia type 1 (MEN1)
S A Forbes, A A Pannett, J H Bassett, et al.
Journal of Medical Genetics
|
February 27, 2004
Germline and de novo mutations in the HRPT2 tumour suppressor gene in familial isolated hyperparathyroidism (FIHP)
A Villablanca, A Calender, L Forsberg, et al.
Clinical Genetics
|
July 4, 2015
Whole-exome sequencing improves the diagnosis yield in sporadic infantile spasm syndrome
S Dimassi, A Labalme, D Ville, et al.
Page
of 9