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Alfonso Massimiliano Ferrara

azienda ospedaliera - universita di padova

H指数:21

被引数:1,948

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Euthyroid hyperthyroxinemia: relevance of albumin and transthyretin genetic variations in a single centre experience

正常甲状腺功能的高甲状腺素血症：白蛋白和甲状腺素结合球蛋白基因变异的相关性——一项单中心经验研究

CLINICA CHIMICA ACTA

IF2.9

2025-06-010

OA

Obstructive azoospermia as the first presentation of Von Hippel-Lindau disease

FRONTIERS IN ONCOLOGY

IF3.3

2023-12-120

OAAI

von Hippel-Lindau disease integrated care pathway: Centralizing, expanding specialists' theatre, and measuring improvement

IF5.1

2022-09-281

PRE

Real-life monocentric, retrospective study on efficacy and tolerability of lenvatinib (Len) in patients (pts) with advanced radioactive iodine-refractory differentiated thyroid cancer (rDTC)

ANNALS OF ONCOLOGY

IF65.4

2021-09-010

OAAI

Structural and microvascular changes of the peripapillary retinal nerve fiber layer in Von Hippel-Lindau disease: an OCT and OCT angiography study

SCIENTIFIC REPORTS

IF3.9

2021-01-089

OAAI

Macular Perfusion Impairment in Von Hippel-Lindau Disease Suggests a Generalized Retinal Vessel Alteration

JOURNAL OF CLINICAL MEDICINE

IF2.9

2020-08-186

OAAI

A Novel Thyroid Hormone Receptor Beta Mutation (G357R) in a Family with Resistance to Thyroid Hormone Beta: Extending the Borders of the Hot Region in the THRB Gene

IF6.7

2019-03-152

PREAI

Preventive medicine of von Hippel-Lindau disease-associated pancreatic neuroendocrine tumors

von hippel-lindau病相关胰腺神经内分泌肿瘤的预防医学

ENDOCRINE-RELATED CANCER

IF4.6

2018-09-0146

OAAI

Krauss, Tobias; Ferrara, Alfonso Massimiliano; Links, Thera P.; Wellner, Ulrich; Bancoss, Irina; Kvachenyuk, Andrey; Gomez de las Heras, Karim Villar; Yukina, Marina Y.; Petrov, Roman; Bullivant, Garrett; von Duecker, Laura; Jadhav, Swati; Ploeckinger, Ursula; Welin, Staffan; Schalin-Jantti, Camilla; Gimm, Oliver; Pfeifer, Marija; Ngeow, Joanne; Hasse-Lazar, Kornelia; Sanso, Gabriela; Qi, Xiaoping; Ugurlu, M. Umit; Diaz, Rene E.; Wohllk, Nelson; Peczkowska, Mariola; Aberle, Jens; Lourenco Jr, Delmar M.; Pereira, Maria A. A.; Fragoso, Maria C. B., V; Hoff, Ana O.; Almeida, Madson Q.; Violante, Alice H. D.; Ouidute, Ana R. P.; Zhang, Zhewei; Recasens, Monica; Robles Diaz, Luis; Kunavisarut, Tada; Wannachalee, Taweesak; Sirinvaravong, Sirinart; Jonasch, Eric; Grozinsky-Glasberg, Simona; Fraenkel, Merav; Beltsevich, Dmitry; Egorov, Viacheslav, I; Bausch, Dirk; Schott, Matthias; Tiling, Nikolaus; Pennelli, Gianmaria; Zschiedrich, Stefan; Daerr, Roland; Ruf, Juri; Denecke, Timm; Link, Karl-Heinrich; Zovato, Stefania; von Dobschuetz, Ernst; Yaremchuk, Svetlana; Amthauer, Holger; Makay, Ozer; Patocs, Attila; Walz, Martin K.; Huber, Tobias B.; Seufert, Jochen; Hellman, Per; Kim, Raymond H.; Kuchinskaya, Ekaterina; Schiavi, Francesca; Malinoc, Angelica; Reisch, Nicole; Jarzab, Barbara; Barontini, Marta; Januszewicz, Andrzej; Shah, Nalini; Young, William F., Jr.; Opocher, Giuseppe; Eng, Charis; Neumann, Hartmut P. H.; Bausch, Birke

A multicenter experience on the prevalence of ARMC5 mutations in patients with primary bilateral macronodular adrenal hyperplasia: from genetic characterization to clinical phenotype

IF2.9

2016-04-1956

PREAI

Inherited defects of thyroxine-binding proteins

甲状腺素结合蛋白的遗传缺陷

BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM

IF6.1

2015-10-0194

OAAI

The Thyroid Hormone Analog DITPA Ameliorates Metabolic Parameters of Male Mice With Mct8 Deficiency

IF3.3

2015-08-3124

OAAI

A Novel Mechanism of Inherited TBG Deficiency: Mutation in a Liver-Specific Enhancer

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

IF5.1

2015-01-0111

OAAI

Placenta Passage of the Thyroid Hormone Analog DITPA to Male Wild-Type and Mct8-Deficient Mice

IF3.3

2014-10-0124

OAAI

A Novel Mutation in the Albumin Gene (R218S) Causing Familial Dysalbuminemic Hyperthyroxinemia in a Family of Bangladeshi Extraction

IF6.7

2014-06-0124

OAAI

Mutations in TAZ/WWTR1, a co-activator of NKX2.1 and PAX8 are not a frequent cause of thyroid dysgenesis

JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION

IF3.5

2014-03-277

PREAI

Mct8-Deficient Mice Have Increased Energy Expenditure and Reduced Fat Mass That Is Abrogated by Normalization of Serum T3 Levels

IF3.3

2013-12-0136

OAAI

Coexistence of THRB and TBG Gene Mutations in a Turkish Family

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

IF5.1

2013-06-016

OAAI

Identification and Functional Characterization of a Novel Mutation in the NKX2-1 Gene: Comparison with the Data in the Literature

IF6.7

2013-06-0127

PREAI

Changes in Thyroid Status During Perinatal Development of MCT8-Deficient Male Mice

IF3.3

2013-05-2159

OA

Homozygous Thyroid Hormone Receptor β-Gene Mutations in Resistance to Thyroid Hormone: Three New Cases and Review of the Literature

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

IF5.1

2012-04-0177

OA