UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 253

Sortiert nach

Composition and sources of aliphatic lipids and sterols in sediments of a tropical island, southern South China Sea: preliminary assessment

Environmental monitoring and assessment, 2013-12, Vol.185 (12), p.10209-10216

2013

Link zum Volltext

Verfügbarkeit prüfen

Consensus Statement on 21-Hydroxylase Deficiency from The Lawson Wilkins Pediatric Endocrine Society and The European Society for Paediatric Endocrinology

The journal of clinical endocrinology and metabolism, 2002-09, Vol.87 (9), p.4048-4053

2002

Link zum Volltext

Verfügbarkeit prüfen

Influence of patients＇ age on functional recovery after transplantation of olfactory ensheathing cells into injured spinal cord injury

Chinese medical journal, 2003-10, Vol.116 (10), p.1488-1491

黄红云陈琳王洪美修波李炳辰王锐张健张峰顾征李荧宋英伦郝伟潘树义孙君昭

2003

Link zum Volltext

Verfügbarkeit prüfen

CONGENITAL ADRENAL HYPERPLASIA

Endocrinology and metabolism clinics of North America, 1997-12, Vol.26 (4), p.853-891

Pang, Songya

1997

Link zum Volltext

Verfügbarkeit prüfen

CONGENITAL ADRENAL HYPERPLASIA OWING TO 3β-HYDROXYSTEROID DEHYDROGENASE DEFICIENCY

Endocrinology and metabolism clinics of North America, 2001-03, Vol.30 (1), p.81-99

Pang, Songya

2001

Link zum Volltext

Verfügbarkeit prüfen

Clinical and functional effects of mutations in the DAX-1 gene in patients with adrenal hypoplasia congenita

The journal of clinical endocrinology and metabolism, 1999-02, Vol.84 (2), p.504-511

1999

Link zum Volltext

Verfügbarkeit prüfen

Newborn screening for congenital adrenal hyperplasia

Pediatric annals, 2003-08, Vol.32 (8), p.516

Pang, Songya

2003

Link zum Volltext

Verfügbarkeit prüfen

Facilitating terminal discharge: fulfilling the hospitalised patient's wish for home death in the final hours

International journal of palliative nursing, 2016-11, Vol.22 (11), p.541

2016

Link zum Volltext

Verfügbarkeit prüfen

The Molecular and Clinical Spectrum of 3β-hydroxysteroid Dehydrogenase Deficiency Disorder

Trends in endocrinology and metabolism, 1998-02, Vol.9 (2), p.82-86

Pang, Songya

1998

Link zum Volltext

Verfügbarkeit prüfen

Predicting potentially functional SNPs in drug-response genes

Pharmacogenomics, 2009-04, Vol.10 (4), p.639-653

2009

Link zum Volltext

Verfügbarkeit prüfen

The G allele of SNP E1/A118G at the mu-opioid receptor gene locus shows genomic evidence of recent positive selection

Pharmacogenomics, 2009-07, Vol.10 (7), p.1101-1109

2009

Link zum Volltext

Verfügbarkeit prüfen

Carriers for type II 3β-hydroxysteroid dehydrogenase (HSD3B2) deficiency can only be identified by HSD3B2 genotype study and not by hormone test

Clinical endocrinology (Oxford), 2003-03, Vol.58 (3), p.323-331

2003

Link zum Volltext

Verfügbarkeit prüfen

Characterization of two novel homozygous missense mutations involving codon 6 and 259 of type II 3β-hydroxysteroid dehydrogenase (3βHSD) gene causing, respectively, nonsalt-wasting and salt-wasting 3βHSD deficiency disorder

The journal of clinical endocrinology and metabolism, 2000-04, Vol.85 (4), p.1678-1685

2000

Link zum Volltext

Verfügbarkeit prüfen

The G allele of SNP E1/A118G at the µµ-opioid receptor gene locus shows genomic evidence of recent positive selection

Pharmacogenomics, 2009-07, Vol.10 (7), p.1101-1109

2009

Link zum Volltext

Verfügbarkeit prüfen

The G allele of SNP E1/A118G at the mu mu -opioid receptor gene locus shows genomic evidence of recent positive selection

Pharmacogenomics, 2009-07, Vol.10 (7), p.1101-1109

2009

Link zum Volltext

Verfügbarkeit prüfen

ROC curve analysis of lesion detectability on phantoms: comparison of digital spot mammography with conventional spot mammography

British journal of radiology, 2001-07, Vol.74 (883), p.621

2001

Link zum Volltext

Verfügbarkeit prüfen

An upper bound on the number of edges of edge-coloring critical graphs with high maximum degree

Discrete mathematics, 2003-09, Vol.271 (1), p.321-325

2003

Link zum Volltext

Verfügbarkeit prüfen

Inherited congenital adrenal hyperplasia in the rabbit is caused by a deletion in the gene encoding cytochrome P450 cholesterol side-chain cleavage enzyme

Endocrinology (Philadelphia), 1993-05, Vol.132 (5), p.1977-1982

1993

Link zum Volltext

Verfügbarkeit prüfen

A new compound heterozygous frameshift mutation in the type II 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD) gene causes salt-wasting 3 beta-HSD deficiency congenital adrenal hyperplasia

The journal of clinical endocrinology and metabolism, 1996-01, Vol.81 (1), p.291-295

1996

Link zum Volltext

Verfügbarkeit prüfen

The relationship between luteinizing hormone and estradiol secretion in female precocious puberty: evaluation by sensitive gonadotropin assays and the leuprolide stimulation test

The journal of clinical endocrinology and metabolism, 1993-04, Vol.76 (4), p.851-856

1993

Link zum Volltext

Verfügbarkeit prüfen

On crustal movement in Mt. Qomolangma area

Science China. Earth sciences, 2002-03, Vol.45 (3), p.233-240

2002

Link zum Volltext

Verfügbarkeit prüfen

Absence of molecular defect in the type II 3β-hydroxysteroid dehydrogenase (3β-HSD) gene in premature pubarche children and hirsute female patients with moderately decreased adrenal 3β-HSD activity

Pediatric research, 1995-06, Vol.37 (6), p.820-824

1995

Link zum Volltext

Verfügbarkeit prüfen

Relevance of biological properties of progestogen of oral contraceptives in treatment of androgen excess symptoms

The journal of clinical endocrinology and metabolism, 1990-07, Vol.71 (1), p.5-7

Pang, S

1990

Link zum Volltext

Verfügbarkeit prüfen

Pulmonary embolism presenting as disseminated intravascular coagulation

Hong Kong medical journal = Xianggang yi xue za zhi, 2002-04, Vol.8 (2), p.142-143

2002

Link zum Volltext

Verfügbarkeit prüfen

Hypothalamic-pituitary-adrenal function following cranial irradiation

Hormone research, 1997, Vol.47 (1), p.9

1997

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 253

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(227)
Mit Volltextzugriff
(228)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(221)
Life Sciences & Biomedicine
(126)
Humans
(94)
Physical Sciences
(79)
Female
(68)
Technology
(58)
Male
(56)
Biological And Medical Sciences
(47)
Medical Sciences
(40)
Physics
(38)
Middle Aged
(33)
Animals
(32)
Exact Sciences And Technology
(32)
Adult
(31)
Aged
(29)
Materials Science
(24)
Engineering
(23)
Materials Science, Multidisciplinary
(23)
Physics, Applied
(22)
Endocrinology & Metabolism
(20)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Composition and sources of aliphatic lipids and sterols in sediments of a tropical island, southern South China Sea: preliminary assessment

Consensus Statement on 21-Hydroxylase Deficiency from The Lawson Wilkins Pediatric Endocrine Society and The European Society for Paediatric Endocrinology

Influence of patients＇ age on functional recovery after transplantation of olfactory ensheathing cells into injured spinal cord injury

CONGENITAL ADRENAL HYPERPLASIA

CONGENITAL ADRENAL HYPERPLASIA OWING TO 3β-HYDROXYSTEROID DEHYDROGENASE DEFICIENCY

Clinical and functional effects of mutations in the DAX-1 gene in patients with adrenal hypoplasia congenita

Newborn screening for congenital adrenal hyperplasia

Facilitating terminal discharge: fulfilling the hospitalised patient's wish for home death in the final hours

The Molecular and Clinical Spectrum of 3β-hydroxysteroid Dehydrogenase Deficiency Disorder

Predicting potentially functional SNPs in drug-response genes

The G allele of SNP E1/A118G at the mu-opioid receptor gene locus shows genomic evidence of recent positive selection

Carriers for type II 3β-hydroxysteroid dehydrogenase (HSD3B2) deficiency can only be identified by HSD3B2 genotype study and not by hormone test

Characterization of two novel homozygous missense mutations involving codon 6 and 259 of type II 3β-hydroxysteroid dehydrogenase (3βHSD) gene causing, respectively, nonsalt-wasting and salt-wasting 3βHSD deficiency disorder

The G allele of SNP E1/A118G at the µµ-opioid receptor gene locus shows genomic evidence of recent positive selection

The G allele of SNP E1/A118G at the mu mu -opioid receptor gene locus shows genomic evidence of recent positive selection

ROC curve analysis of lesion detectability on phantoms: comparison of digital spot mammography with conventional spot mammography

An upper bound on the number of edges of edge-coloring critical graphs with high maximum degree

Inherited congenital adrenal hyperplasia in the rabbit is caused by a deletion in the gene encoding cytochrome P450 cholesterol side-chain cleavage enzyme

A new compound heterozygous frameshift mutation in the type II 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD) gene causes salt-wasting 3 beta-HSD deficiency congenital adrenal hyperplasia

The relationship between luteinizing hormone and estradiol secretion in female precocious puberty: evaluation by sensitive gonadotropin assays and the leuprolide stimulation test

On crustal movement in Mt. Qomolangma area

Absence of molecular defect in the type II 3β-hydroxysteroid dehydrogenase (3β-HSD) gene in premature pubarche children and hirsute female patients with moderately decreased adrenal 3β-HSD activity

Relevance of biological properties of progestogen of oral contraceptives in treatment of androgen excess symptoms

Pulmonary embolism presenting as disseminated intravascular coagulation

Hypothalamic-pituitary-adrenal function following cranial irradiation

Suchergebnisse filtern