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Mutations in the Desert hedgehog (DHH) Gene in Patients with 46,XY Complete Pure Gonadal Dysgenesis

The journal of clinical endocrinology and metabolism, 2004-09, Vol.89 (9), p.4480-4483

2004

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Knowledge of appropriate foods and beverages needed for weight loss and diet of patients in an Obesity Clinic

European journal of clinical nutrition, 2015-01, Vol.69 (1), p.68-72

2015

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A heterozygous mutation in the desert hedgehog gene in patients with mixed gonadal dysgenesis

Molecular human reproduction, 2005-11, Vol.11 (11), p.833-836

2005

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No evidence of mutations in the P450 aromatase gene in patients with polycystic ovary syndrome

Human reproduction (Oxford), 2005-04, Vol.20 (4), p.965-969

2005

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Full-length SRY protein is essential for DNA binding

Molecular human reproduction, 2008-06, Vol.14 (6), p.325-330

2008

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Genetic Analysis in Patients With Kallmann Syndrome: Coexistence of Mutations in Prokineticin Receptor 2 and KAL1

Journal of andrology, 2009-01, Vol.30 (1), p.41-45

2009

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A novel homozygous mutation in the second transmembrane domain of the gonadotrophin releasing hormone receptor gene

Clinical endocrinology (Oxford), 2001-04, Vol.54 (4), p.493-498

2001

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A preponderance of circulating basic isoforms is associated with decreased plasma half-life and biological to immunological ratio of gonadotropin-releasing hormone-releasable luteinizing hormone in obese men

The journal of clinical endocrinology and metabolism, 2000-12, Vol.85 (12), p.4603-4610

2000

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Changes in the biological:immunological ratio of basal and GnRH-releasable FSH during the follicular, pre-ovulatory and luteal phases of the human menstrual cycle

Human reproduction (Oxford), 2001-08, Vol.16 (8), p.1611-1618

2001

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Charge-carrier transmission across twins in graphene

Journal of physics. Condensed matter, 2020-10, Vol.32 (42), p.425003-425003

2020

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Regulation of follicle-stimulating and luteinizing hormone receptor signaling by “regulator of G protein signaling” proteins

Endocrine, 2004, Vol.25 (1), p.49-54

2004

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Polymorphic changes in the KAL1 gene: not all of them should be classified as polymorphisms

Journal of endocrinological investigation, 2004-09, Vol.27 (8), p.765-769

2004

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Diffusive molecular dynamics simulations of lithiation of silicon nanopillars

Journal of the mechanics and physics of solids, 2018-06, Vol.115, p.123-141

2018

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Mutations of the 5α-reductase Type 2 gene in eight Mexican patients from six different pedigrees with 5α-reductase-2 deficiency

Clinical endocrinology (Oxford), 1997-02, Vol.46 (2), p.155-160

1997

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Two SRY-negative XX male brothers without genital ambiguity

Human genetics, 1997-10, Vol.100 (5-6), p.606-610

1997

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Basal and gonadotropin-releasing hormone-releasable serum follicle-stimulating hormone charge isoform distribution and in vitro biological-to-immunological ratio in male puberty

Endocrine, 2004-03, Vol.23 (2-3), p.189-198

2004

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Renal abnormalities in patients with Kallmann syndrome

BJU international, 1999-03, Vol.83 (4), p.383-386

1999

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Eight novel mutations of the androgen receptor gene in patients with androgen insensitivity syndrome

Journal of human genetics, 2001-10, Vol.46 (10), p.560-565

2001

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Shear localization as a mesoscopic stress-relaxation mechanism in fused silica glass at high strain rates

Journal of the mechanics and physics of solids, 2020-07, Vol.140, p.103940, Article 103940

2020

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Contiguous gene syndrome due to deletion of the first three exons of the Kallmann gene and complete deletion of the steroid sulphatase gene

Clinical endocrinology (Oxford), 1998-06, Vol.48 (6), p.713-718

1998

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Spontaneous twinning as an accommodation mechanism in monolayer graphene

European journal of mechanics, A, Solids, 2020-03, Vol.80, p.103923, Article 103923

2020

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More in-vitro bioactive, shorter-lived human chorionic gonadotrophin charge isoforms increase at the end of the first and during the third trimesters of gestation

Molecular human reproduction, 1996-09, Vol.2 (9), p.643-650

1996

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An atypical contiguous gene syndrome: molecular studies in a family with X-linked Kallmann's syndrome and X-linked ichthyosis

Clinical endocrinology (Oxford), 1999-02, Vol.50 (2), p.157-162

1999

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Identification of Three Novel Mutations in the KAL1 Gene in Patients with Kallmann Syndrome

The journal of clinical endocrinology and metabolism, 2002-06, Vol.87 (6), p.2589-2592

2002

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A mutation in the 5' non-high mobility group box region of the SRY gene in patients with Turner syndrome and Y mosaicism

The journal of clinical endocrinology and metabolism, 2000-05, Vol.85 (5), p.1908-1911

2000

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Mutations in the Desert hedgehog (DHH) Gene in Patients with 46,XY Complete Pure Gonadal Dysgenesis

Knowledge of appropriate foods and beverages needed for weight loss and diet of patients in an Obesity Clinic

A heterozygous mutation in the desert hedgehog gene in patients with mixed gonadal dysgenesis

No evidence of mutations in the P450 aromatase gene in patients with polycystic ovary syndrome

Full-length SRY protein is essential for DNA binding

Genetic Analysis in Patients With Kallmann Syndrome: Coexistence of Mutations in Prokineticin Receptor 2 and KAL1

A novel homozygous mutation in the second transmembrane domain of the gonadotrophin releasing hormone receptor gene

A preponderance of circulating basic isoforms is associated with decreased plasma half-life and biological to immunological ratio of gonadotropin-releasing hormone-releasable luteinizing hormone in obese men

Changes in the biological:immunological ratio of basal and GnRH-releasable FSH during the follicular, pre-ovulatory and luteal phases of the human menstrual cycle

Charge-carrier transmission across twins in graphene

Regulation of follicle-stimulating and luteinizing hormone receptor signaling by “regulator of G protein signaling” proteins

Polymorphic changes in the KAL1 gene: not all of them should be classified as polymorphisms

Diffusive molecular dynamics simulations of lithiation of silicon nanopillars

Mutations of the 5α-reductase Type 2 gene in eight Mexican patients from six different pedigrees with 5α-reductase-2 deficiency

Two SRY-negative XX male brothers without genital ambiguity

Basal and gonadotropin-releasing hormone-releasable serum follicle-stimulating hormone charge isoform distribution and in vitro biological-to-immunological ratio in male puberty

Renal abnormalities in patients with Kallmann syndrome

Eight novel mutations of the androgen receptor gene in patients with androgen insensitivity syndrome

Shear localization as a mesoscopic stress-relaxation mechanism in fused silica glass at high strain rates

Contiguous gene syndrome due to deletion of the first three exons of the Kallmann gene and complete deletion of the steroid sulphatase gene

Spontaneous twinning as an accommodation mechanism in monolayer graphene

More in-vitro bioactive, shorter-lived human chorionic gonadotrophin charge isoforms increase at the end of the first and during the third trimesters of gestation

An atypical contiguous gene syndrome: molecular studies in a family with X-linked Kallmann's syndrome and X-linked ichthyosis

Identification of Three Novel Mutations in the KAL1 Gene in Patients with Kallmann Syndrome

A mutation in the 5' non-high mobility group box region of the SRY gene in patients with Turner syndrome and Y mosaicism

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