Normal male sexual differentiation and aetiology of disorders of sex development.
about
Endocrine control of spermatogenesis: Role of FSH and LH/ testosteroneAnti-Müllerian hormone as a marker of steroid and gonadotropin action in the testis of children and adolescents with disorders of the gonadal axisSpreading the clinical window for diagnosing fetal-onset hypogonadism in boysA newborn with ambiguous genitalia and a complex X;Y rearrangementMECHANISMS IN ENDOCRINOLOGY: The sexually dimorphic role of androgens in human metabolic disease.Disorders of sex development: new genes, new concepts.Female form of persistent mullerian duct syndrome: Rare entity.Quantitative Proteomics Reveals the Essential Roles of Stromal Interaction Molecule 1 (STIM1) in the Testicular Cord Formation in Mouse Testis.Indirect inguinal hernia with uterine tissue in a male: A case of persistent Mullerian duct syndrome and literature reviewSerum AMH in Physiology and Pathology of Male Gonads.Anti-müllerian hormone and its clinical use in pediatrics with special emphasis on disorders of sex development.408 Cases of Genital Ambiguity Followed by Single Multidisciplinary Team during 23 Years: Etiologic Diagnosis and Sex of Rearing.Male hypogonadism: an extended classification based on a developmental, endocrine physiology-based approach.When hormone defects cannot explain it: malformative disorders of sex development.Putting the pieces together: cryptorchidism - do we know everything?Concepts and Updates in the Evaluation and Diagnosis of Common Disorders of Sexual Development.Disorders of sex development presenting as unilateral cryptorchidism.Gonadotrophin secretion pattern in anorchid boys from birth to pubertal age: pathophysiological aspects and diagnostic usefulness.Sexually antagonistic epigenetic marks that canalize sexually dimorphic development.Serum anti-mullerian hormone and all-cause mortality in men.The AMH genotype (rs10407022 T>G) is associated with circulating AMH levels in boys, but not in girls.A novel mutation of AMH in three siblings with persistent Mullerian duct syndrome.Maternal uniparental disomy for chromosome 6 in a patient with IUGR, ambiguous genitalia, and persistent mullerian structures.The Evaluation of Cases with Y-Chromosome Gonadal Dysgenesis: Clinical Experience over 18 Years.A perivascular niche for multipotent progenitors in the fetal testis
P2860
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P2860
Normal male sexual differentiation and aetiology of disorders of sex development.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on April 2011
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Normal male sexual differentiation and aetiology of disorders of sex development.
@en
Normal male sexual differentiation and aetiology of disorders of sex development.
@nl
type
label
Normal male sexual differentiation and aetiology of disorders of sex development.
@en
Normal male sexual differentiation and aetiology of disorders of sex development.
@nl
prefLabel
Normal male sexual differentiation and aetiology of disorders of sex development.
@en
Normal male sexual differentiation and aetiology of disorders of sex development.
@nl
P1476
Normal male sexual differentiation and aetiology of disorders of sex development
@en
P2093
Romina P Grinspon
P304
P356
10.1016/J.BEEM.2010.08.013
P577
2011-04-01T00:00:00Z