21
TITLE: Absence of Central Circadian Pacemaker Abnormalities in Humans With Loss of Function Mutation in Prokineticin 2
AUTHORS: Ravikumar Balasubramanian; Daniel A Cohen; Elizabeth B Klerman; Duarte Pignatelli; Janet E Hall; Andrew A Dwyer; Charles A Czeisler; Nelly Pitteloud; William F Crowley;
PUBLISHED: 2014, SOURCE: JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, VOLUME: 99, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef: 5
22
TITLE: The polycystic ovary syndrome: a position statement from the European Society of Endocrinology
AUTHORS: Gerard Conway; Didier Dewailly; Evanthia Diamanti Kandarakis; Hector F Escobar Morreale; Stephen Franks; Alessandra Gambineri; Fahrettin Kelestimur; Djuro Macut; Dragan Micic; Renato Pasquali; Marija Pfeifer; Duarte Pignatelli; Michel Pugeat; Bulent O Yildiz;
PUBLISHED: 2014, SOURCE: EUROPEAN JOURNAL OF ENDOCRINOLOGY, VOLUME: 171, ISSUE: 4
INDEXED IN: Scopus WOS CrossRef: 311
23
TITLE: European survey of diagnosis and management of the polycystic ovary syndrome: results of the ESE PCOS Special Interest Group's Questionnaire
AUTHORS: Gerard Conway; Didier Dewailly; Evanthia Diamanti Kandarakis; Hector F Escobar Morreale; Steven Franks; Alessandra Gambineri; Fahrettin Kelestimur; Djuro Macut; Dragan Micic; Renato Pasquali; Marija Pfeifer; Duarte Pignatelli; Michel Pugeat; Bulent O Yildiz;
PUBLISHED: 2014, SOURCE: EUROPEAN JOURNAL OF ENDOCRINOLOGY, VOLUME: 171, ISSUE: 4
INDEXED IN: Scopus WOS CrossRef: 45
25
TITLE: Responsiveness to a Physiological Regimen of GnRH Therapy and Relation to Genotype in Women With Isolated Hypogonadotropic Hypogonadism
AUTHORS: Brent S Abel; Natalie D Shaw; Jenifer M Brown; Judith M Adams; Teresa Alati; Kathryn A Martin; Nelly Pitteloud; Stephanie B Seminara; Lacey Plummer; Duarte Pignatelli; William F Crowley; Corrine K Welt; Janet E Hall;
PUBLISHED: 2013, SOURCE: JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, VOLUME: 98, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef: 20
27
TITLE: Cyclosporine or Tacrolimus in Pediatric Kidney Transplantation: Single-Center experience  Full Text
AUTHORS: Pignatelli, D; Barroso, L; Gomes, A; Silva, JE; Almeida, M;
PUBLISHED: 2011, SOURCE: PEDIATRIC NEPHROLOGY, VOLUME: 26, ISSUE: 8
INDEXED IN: WOS
28
TITLE: Mutational Characterization of Steroid 21-Hydroxylase Gene in Portuguese patients with Congenital Adrenal Hyperplasia
AUTHORS: Marques, CJ ; Pignatelli, D; Carvalho, B; Barcelo, J; Almeida, AC; Fernandes, S; Witchel, SF; Sousa, M ; Oliveira, MJ; Freitas, P ; Fontoura, M ; Carvalho, D ; Barros, A ; Carvalho, F ;
PUBLISHED: 2010, SOURCE: EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES, VOLUME: 118, ISSUE: 8
INDEXED IN: Scopus WOS CrossRef: 9
29
TITLE: The phenotype of hirsute women: a comparison of polycystic ovary syndrome and 21-hydroxylase-deficient nonclassic adrenal hyperplasia
AUTHORS: Marita Pall; Ricardo Azziz; Jorge Beires; Duarte Pignatelli;
PUBLISHED: 2010, SOURCE: FERTILITY AND STERILITY, VOLUME: 94, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef: 69
30
TITLE: Melanocortin 5 receptor activates ERK1/2 through a PI3K-regulated signaling mechanism  Full Text
AUTHORS: Adriana R Rodrigues ; Duarte Pignatelli; Almeida, H ; Alexandra M Gouveia ;
PUBLISHED: 2009, SOURCE: MOLECULAR AND CELLULAR ENDOCRINOLOGY, VOLUME: 303, ISSUE: 1-2
INDEXED IN: Scopus WOS CrossRef: 24
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