FERLIN, ALBERTO
 Distribuzione geografica
Continente #
NA - Nord America 11713
EU - Europa 2070
AS - Asia 1344
Continente sconosciuto - Info sul continente non disponibili 36
AF - Africa 11
OC - Oceania 3
Totale 15177
Nazione #
US - Stati Uniti d'America 11705
UA - Ucraina 1482
CN - Cina 1316
DE - Germania 292
IT - Italia 122
GB - Regno Unito 90
SE - Svezia 41
EU - Europa 36
BE - Belgio 14
TR - Turchia 11
MU - Mauritius 10
FR - Francia 7
CA - Canada 6
FI - Finlandia 6
RU - Federazione Russa 6
IN - India 5
NL - Olanda 4
AU - Australia 3
CZ - Repubblica Ceca 3
HK - Hong Kong 3
IR - Iran 3
HN - Honduras 2
VN - Vietnam 2
BG - Bulgaria 1
CY - Cipro 1
HU - Ungheria 1
JP - Giappone 1
PK - Pakistan 1
RO - Romania 1
SG - Singapore 1
ZA - Sudafrica 1
Totale 15177
Città #
Fairfield 2462
Woodbridge 1411
Jacksonville 1257
Ashburn 1126
Seattle 987
Cambridge 986
Houston 924
Wilmington 779
Princeton 556
Nanjing 381
Ann Arbor 312
Chandler 301
Des Moines 133
Nanchang 126
Changsha 114
Dearborn 103
Shenyang 92
San Diego 91
Beijing 90
Hebei 83
Tianjin 76
Jiaxing 70
Hangzhou 46
Napoli 43
Boardman 41
Jinan 41
Kunming 33
Ningbo 30
Falls Church 23
Guangzhou 22
Brescia 20
Zhengzhou 20
Norwalk 17
Lanzhou 16
Taizhou 14
Brussels 13
Changchun 10
Haikou 10
Taiyuan 10
Kocaeli 7
San Francisco 7
Fuzhou 6
Orange 6
San Cesareo 6
Hefei 5
London 5
Redmond 5
Brooklyn 4
Helsinki 4
New York 4
Padova 4
Redwood City 4
Rome 4
Brindisi 3
Brno 3
Canberra 3
Milan 3
Auburn Hills 2
Bournemouth 2
Central 2
Chicago 2
Fars 2
Hanover 2
Indiana 2
La Ceiba 2
Los Angeles 2
Montichiari 2
Ottawa 2
Paterno 2
Qingdao 2
Toronto 2
Treviso 2
Alice 1
Augusta 1
Berlin 1
Budapest 1
Chongqing 1
Cremona 1
Genova 1
Grosio 1
Hendon 1
Islamabad 1
Jinhua 1
Kish 1
Krasnoyarsk 1
Leawood 1
Marcaria 1
Markham 1
Nagold 1
Nanning 1
Omsk 1
Pavia 1
Phoenix 1
Pretoria 1
Quzhou 1
Sant'anastasia 1
Schoten 1
Shanghai 1
Singapore 1
Yellow Springs 1
Totale 13010
Nome #
Diagnostics of CFTR-negative patients with congenital bilateral absence of vas deferens: which mutations are of most interest? 122
Meta-analysis of five genome-wide association studies identifies multiple new loci associated with testicular germ cell tumor 100
Y-chromosome microdeletions are not associated with SHOX haploinsufficiency 97
Calcium-sensing receptor polymorphisms increase the risk of osteoporosis in ageing males 96
Mechanism of Human Papillomavirus Binding to Human Spermatozoa and Fertilizing Ability of Infected Spermatozoa 95
Polymorphisms associated with the DAZ genes on the human Y chromosome 93
Penile doppler ultrasound predicts cardiovascular events in men with erectile dysfunction 92
Y-CHROMOSOME HAPLOGRUPS AND SUSCEPTIBILITY TO AZOOSPERMIA FACTOR C MICRODELETION IN AN ITALIAN POPULATION 91
Selenium supplementation in patients with subclinical hypothyroidism affected by autoimmune thyroiditis: Results of the SETI study 91
Association of partial AZFc region deletions with spermatogenic impairment and male infertility. 88
Male infertility: role of genetic background 88
Relaxin and insulin-like peptide 3 in the musculoskeletal system: From bench to bedside 88
Contemporary genetics-based diagnostics of male infertility 88
A novel approach for the analysis of DAZ gene copy number in severely idiopathic infertile men 87
Use of recombinant human follicle-stimulating hormone in the treatment of male factor infertility 86
Treatment with human, recombinant FSH improves sperm DNA fragmentation in idiopathic infertile men depending on the FSH receptor polymorphism p.N680S: A pharmacogenetic study 86
Characteristics of a nationwide cohort of patients presenting with isolated hypogonadotropic hypogonadism (IHH) 86
Testis transcriptome analysis in male infertility: new insight on the pathogenesis of oligo-azoospermia in cases with and without AZFc microdeletion 86
Insulin-like factor 3 as a marker of testicular function in obese men 85
Y chromosome haplogroups and susceptibility to testicular cancer 85
Ultrasound microvascular blood flow evaluation: A new tool for the management of thyroid nodule? 84
Semen quality and fertility. 82
Telomere length: lights and shadows on their role in human reproduction 82
Androgen receptor is expressed in both X- and Y-carrier human spermatozoa 81
Androgen receptor gene CAG and GGC repeat lengths in cryptorchidism 80
The use of follicle stimulating hormone (FSH) for the treatment of the infertile man: position statement from the Italian Society of Andrology and Sexual Medicine (SIAMS) 79
Use of intracytoplasmic sperm injection in severe male factor infertility 79
Doppler ultrasound of the testis in azoospermic subjects as a parameter of testicular function. 79
Novel Insights on Testicular Volume and Testosterone Replacement Therapy in Klinefelter Patients Undergoing Testicular Sperm Extraction. A Retrospective Clinical Study 78
Uncarboxylated Osteocalcin Stimulates 25-Hydroxy Vitamin D Production in Leydig Cell Line Through a GPRC6a-Dependent Pathway 78
Non-neural phenotype of spinal and bulbar muscular atrophy: Results from a large cohort of Italian patients 78
Protective Role of Testicular Hormone INSL3 From Atrophy and Weakness in Skeletal Muscle 78
Risk behaviours and alcohol in adolescence are negatively associated with testicular volume: results from the Amico-Andrologo survey 78
Warning note on male infertility treatment. 77
Role of familiarity versus interleukin-1 genes cluster polymorphisms in chronic periodontitis 77
Outcomes of androgen replacement therapy in adult male hypogonadism: recommendations from the Italian society of endocrinology 77
Variants in KITLG predispose to testicular germ cell cancer independently from spermatogenic function. 77
Thyroid function in Klinefelter syndrome: a multicentre study from KING group 77
INSL3/RXFP2 signaling in testicular descent. 76
The Klinefelter syndrome: Current management and research challenges 76
Genetics of male infertility 76
E2F1 copy number variations contribute to spermatogenic impairment and cryptorchidism by increasing susceptibility to heat stress 76
Negative Association Between Sclerostin and INSL3 in Isolated Human Osteocytes and in Klinefelter Syndrome: New Hints for Testis-Bone Crosstalk 75
Mutations in the insulin-like factor 3 receptor are associated with osteoporosis 75
Toward a pharmacogenetic approach to male infertility: polymorphism of follicle-stimulating hormone beta-subunit promoter 75
Prognostic value of Y deletion analysis - The role of current methods 75
Analysis of meiosis in intratesticular germ cells from subjects affected by classic Klinefelter's syndrome. 75
Clinical implication of endothelial progenitor cells 75
Case report: high fertilization rate in conventional in-vitro fertilization utilizing spermatozoa from an oligozoospermic subject presenting microdeletions of the Y chromosome long arm. 75
D-Aspartic acid stimulates steroidogenesis through the delay of LH receptor internalization in a mammalian Leydig cell line 75
RXFP1 is expressed on the sperm acrosome, and relaxin stimulates the acrosomal reaction of human spermatozoa. 75
Treatment of male idiopathic infertility with recombinant human follicle-stimulating hormone: a prospective, controlled, randomized clinical study 74
Offspring conceived by intracytoplasmic sperm injection 74
A possible association of a human tektin-t gene mutation (A229V) with isolated non-syndromic asthenozoospermia: Case Report 74
Spermatogenesis in Klinefelter syndrome. 74
Effects of endogenous FSH on normal human spermatogenesis in adults 74
INSL3 in the muscolo-skeletal system 74
Y chromosome microdeletions and alterations of spermatogenesis 73
Mutational screening of NR5A1 gene encoding steroidogenic factor 1 in cryptorchidism and male factor infertility and functional analysis of seven undescribed mutations 73
Testicular Contrast Harmonic Imaging to Evaluate Intratesticular Perfusion Alterations in Patients With Varicocele 73
Mutations in dynein genes in patients affected by isolated non-syndromic asthenozoospermia 73
Sperm recovery and ICSI outcomes in Klinefelter syndrome: a systematic review and meta-analysis 73
Kallmann's syndrome and normosmic isolated hypogonadotropic hypogonadism: two largely overlapping manifestations of one rare disorder 73
Absence of testicular DAZ gene expression in idiopathic severe testiculopathies. 72
Diagnostic and clinical features in azoospermia. 72
Y chromosome microdeletions in infertile men with varicocele 72
Androgen receptor gene CAG and GGC repeat lengths in idiopathic male infertility 72
Androgens stimulate endothelial progenitor cells through an androgen receptor-mediated pathway 71
Prostate volume and growth during testosterone replacement therapy is related to visceral obesity in Klinefelter syndrome 71
Molecular karyotyping of human single sperm by array- comparative genomic hybridization 71
Role of vitamin D levels and vitamin D supplementation on bone mineral density in Klinefelter syndrome 71
New genetic markers for male infertility 71
New understandings of the genetic basis of isolated idiopathic central hypogonadism. 71
Klinefelter syndrome: cardiovascular abnormalities and metabolic disorders 71
Role of relaxin in human osteoclastogenesis. 70
Novel insulin-like 3 (INSL3) gene mutation associated with human cryptorchidism 70
Different insulin-like 3 (INSL3) gene mutations not associated with human cryptorchidism 70
Identification of functional binding sites for progesterone in rat Leydig cell plasma membrane. 70
Reduced artery diameters in Klinefelter syndrome 70
Hormonal and genetic control of testicular descent 70
Genetic causes of male infertility 70
Evidence for stimulatory role of follicle-stimulating hormone on the spermatogonial population in adult males. 70
Role of estrogen receptors in menstrual cycle-related neoangiogenesis and their influence on endothelial progenitor cell physiology 70
Radiofrequency ablation of functioning and non-functioning thyroid nodules: a single institution 12-month survey 70
Hypovitaminosis D is associated with lower urinary tract symptoms and benign prostate hyperplasia in type 2 diabetes 69
How the human spermatozoa sense the oocyte: a new role of SDF1-CXCR4 signalling. 69
Osteocalcin, a bone-derived hormone with important andrological implications 69
Insulin-like factor 3: a novel circulating hormone of testicular origin in humans 69
Analysis of single nucleotide polymorphisms of FSH receptor gene suggests association with testicular cancer susceptibility 69
Testicular cancer and HPV semen infection 69
Polymorphism rs2274911 of GPRC6A as a Novel Risk Factor for Testis Failure 69
Improvements in human sperm quality by long-term in vitro co-culture with isolated porcine Sertoli cells. 69
Progress in the development of childhood cancer therapy 68
Insulin-like factor 3 gene mutations in testicular dysgenesis syndrome: clinical and functional characterization 68
Relationship between vascular damage degrees and endothelial progenitor cells in patients with erectile dysfunction: Effect of vardenafil administration and PDE5 expression in the bone marrow 68
Genetic Alterations Associated With Cryptorchidism 68
PDE-5 inhibitor, Vardenafil, increases circulating progenitor cells in humans. 68
Male infertility caused by a de novo partial deletion of the DAZ cluster on the Y chromosome 68
Osteocalcin and Sex Hormone Binding Globulin Compete on a Specific Binding Site of GPRC6A 68
Adherence to Levothyroxine Treatment Among Patients With Hypothyroidism: A Northeastern Italian Survey 68
Totale 7693
Categoria #
all - tutte 32598
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 32598


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2017/2018587 0000 00 0239 20301387
2018/20192434 17286 25137 80261 8351722628
2019/20205807 932182232675 364692 535649 435624129358
2020/20213855 76380110408 450447 169440 349519344163
2021/20221951 11045040149 4564 166188 110144163322
2022/2023682 318102187 1650 00 0000
Totale 15329