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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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A novel mutation of the insulin-like 3 gene in patients with cryptorchidism

Journal of human genetics, 2003-02, Vol.48 (2), p.86-90

2003

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A recurrent missense mutation in the KAL gene in patients with X-linked Kallmann's syndrome

The journal of clinical endocrinology and metabolism, 1998-05, Vol.83 (5), p.1650-1653

1998

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Evidence for genetic heterogeneity in male pseudohermaphroditism due to Leydig cell hypoplasia

The journal of clinical endocrinology and metabolism, 1999-10, Vol.84 (10), p.3803-3806

1999

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A reliable endocrine test with human menopausal gonadotropins for diagnosis of true hermaphroditism in early infancy

The journal of clinical endocrinology and metabolism, 1998-10, Vol.83 (10), p.3523-3526

1998

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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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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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Incomplete regression of Müllerian ducts in the androgen insensitivity syndrome

Fertility and sterility, 1990-06, Vol.53 (6), p.1024-1028

1990

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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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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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Changes in the responsiveness of prolactin secretion to dopaminergic blockade and TRH stimulation throughout sexual maturation in men

Psychoneuroendocrinology, 1990, Vol.15 (4), p.279-286

1990

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CHANGES IN THE RESPONSIVENESS OF LUTEINIZING HORMONE SECRETION TO INFUSION OF THE OPIOID ANTAGONIST NALOXONE THROUGHOUT MALE SEXUAL MATURATION

Clinical endocrinology (Oxford), 1988-07, Vol.29 (1), p.17-28

1988

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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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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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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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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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Renal abnormalities in patients with Kallmann syndrome

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

1999

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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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Pituitary–testicular axis function, biological to immunological ratio and charge isoform distribution of pituitary LH in male rats with experimental diabetes

General and comparative endocrinology, 2009-05, Vol.161 (3), p.304-312

2009

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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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Low serum testosterone/dihydrotestosterone ratio in patients with pancreatic carcinoma

Pancreas, 1987, Vol.2 (6), p.684

1987

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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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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

A novel mutation of the insulin-like 3 gene in patients with cryptorchidism

A recurrent missense mutation in the KAL gene in patients with X-linked Kallmann's syndrome

Evidence for genetic heterogeneity in male pseudohermaphroditism due to Leydig cell hypoplasia

A reliable endocrine test with human menopausal gonadotropins for diagnosis of true hermaphroditism in early infancy

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

Identification of three novel mutations in the KAL1 gene in patients with Kallmann syndrome

Incomplete regression of Müllerian ducts in the androgen insensitivity syndrome

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

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

Changes in the responsiveness of prolactin secretion to dopaminergic blockade and TRH stimulation throughout sexual maturation in men

CHANGES IN THE RESPONSIVENESS OF LUTEINIZING HORMONE SECRETION TO INFUSION OF THE OPIOID ANTAGONIST NALOXONE THROUGHOUT MALE SEXUAL MATURATION

Two SRY-negative XX male brothers without genital ambiguity

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

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

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

Renal abnormalities in patients with Kallmann syndrome

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

Pituitary–testicular axis function, biological to immunological ratio and charge isoform distribution of pituitary LH in male rats with experimental diabetes

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

Low serum testosterone/dihydrotestosterone ratio in patients with pancreatic carcinoma

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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