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Electroconvulsive therapy for catatonia: treatment characteristics and outcomes in 27 patients

The journal of ECT, 2010-12, Vol.26 (4), p.248

2010

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A retrospective study of 34 catatonic patients: analysis of clinical care and treatment

General hospital psychiatry, 2010-11, Vol.32 (6), p.631-635

2010

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A new locus for postaxial polydactyly type A B on chromosome 7q21-q34

European journal of human genetics : EJHG, 2003-05, Vol.11 (5), p.409-415

2003

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Phenotypic Characteristics of Male Subfertility and Its Familial Occurrence

Journal of andrology, 2004-09, Vol.25 (5), p.819-823

2004

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Are myo-inositol, glucose and zinc concentrations in amniotic fluid of fetuses with spina bifida different from controls?

Early human development, 2003-02, Vol.71 (1), p.1-8

2003

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Familial oligoasthenoteratozoospermia: evidence of autosomal dominant inheritance with sex-limited expression

Fertility and sterility, 2002-02, Vol.77 (2), p.415-418

2002

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Decreased fertilization rate and embryo quality after ICSI in oligozoospermic men with microdeletions in the azoospermia factor c region of the Y chromosome

Human reproduction (Oxford), 2001-02, Vol.16 (2), p.289-292

2001

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Physiology: Dazla: An important candidate gene in male subfertility?

Journal of assisted reproduction and genetics, 2001-07, Vol.18 (7), p.395-399

2001

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Underestimation of Subfertility Among Relatives When Using a Family History: Taboo Bias

Journal of andrology, 2003-03, Vol.24 (2), p.285-288

2003

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Dichotomy of psychiatric and somatic emergency care; fundamental flaw should be addressed

Nederlands tijdschrift voor geneeskunde, 2015, Vol.159, p.A9151

2015

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DAZLA: An important candidate gene in male subfertility?

Journal of assisted reproduction and genetics, 2001-07, Vol.18 (7), p.395-399

2001

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Isochromosome 18q in a girl with holoprosencephaly, DiGeorge anomaly, and streak ovaries

American journal of medical genetics, 1993-08, Vol.47 (1), p.85-88

1993

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Recognition of psychiatrically vulnerable pregnant women

Nederlands tijdschrift voor geneeskunde, 2010, Vol.154 (47), p.A2344

2010

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Trismus-pseudocamptodactyly syndrome is caused by recurrent mutation of MYH8

American journal of medical genetics. Part A, 2006-11, Vol.140A (22), p.2387-2393

2006

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Microdeletions of the Y chromosome and intracytoplasmic sperm injection: from gene to clinic

Human reproduction (Oxford), 1997-04, Vol.12 (4), p.687-691

1997

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Limb Mammary Syndrome: A New Genetic Disorder with Mammary Hypoplasia, Ectrodactyly, and Other Hand/Foot Anomalies Maps to Human Chromosome 3q27

American journal of human genetics, 1999-02, Vol.64 (2), p.538-546

1999

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Reproductive decisions of men with microdeletions of the Y chromosome: the role of genetic counselling

Human reproduction (Oxford), 1999-08, Vol.14 (8), p.2166-2169

1999

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Mutation Frequency of Cystic Fibrosis Transmembrane Regulator is not Increased in Oligozoospermic Male Candidates For Intracytoplasmic Sperm Injection

Fertility and sterility, 1998-05, Vol.69 (5), p.899-903

1998

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Screening male intracytoplasmic sperm injection candidates for mutations of the follicle stimulating hormone receptor gene

Human reproduction (Oxford), 1998-08, Vol.13 (8), p.2098-2101

1998

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Does intracytoplasmic sperm injection lead to a rise in the frequency of microdeletions in the AZFc region of the Y chromosome in future generations?

Human reproduction (Oxford), 1998-10, Vol.13 (10), p.2808-2811

1998

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Another patient with an interstitial deletion of chromosome 9: case report and a review of six cases with del(9)(q22q32)

Journal of medical genetics, 1994-02, Vol.31 (2), p.156-158

1994

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Electroconvulsive therapy for catatonia: treatment characteristics and outcomes in 27 patients

A retrospective study of 34 catatonic patients: analysis of clinical care and treatment

A new locus for postaxial polydactyly type A B on chromosome 7q21-q34

Phenotypic Characteristics of Male Subfertility and Its Familial Occurrence

Are myo-inositol, glucose and zinc concentrations in amniotic fluid of fetuses with spina bifida different from controls?

Familial oligoasthenoteratozoospermia: evidence of autosomal dominant inheritance with sex-limited expression

Decreased fertilization rate and embryo quality after ICSI in oligozoospermic men with microdeletions in the azoospermia factor c region of the Y chromosome

Physiology: Dazla: An important candidate gene in male subfertility?

Underestimation of Subfertility Among Relatives When Using a Family History: Taboo Bias

Dichotomy of psychiatric and somatic emergency care; fundamental flaw should be addressed

DAZLA: An important candidate gene in male subfertility?

Isochromosome 18q in a girl with holoprosencephaly, DiGeorge anomaly, and streak ovaries

Recognition of psychiatrically vulnerable pregnant women

Trismus-pseudocamptodactyly syndrome is caused by recurrent mutation of MYH8

Microdeletions of the Y chromosome and intracytoplasmic sperm injection: from gene to clinic

Limb Mammary Syndrome: A New Genetic Disorder with Mammary Hypoplasia, Ectrodactyly, and Other Hand/Foot Anomalies Maps to Human Chromosome 3q27

Reproductive decisions of men with microdeletions of the Y chromosome: the role of genetic counselling

Mutation Frequency of Cystic Fibrosis Transmembrane Regulator is not Increased in Oligozoospermic Male Candidates For Intracytoplasmic Sperm Injection

Screening male intracytoplasmic sperm injection candidates for mutations of the follicle stimulating hormone receptor gene

Does intracytoplasmic sperm injection lead to a rise in the frequency of microdeletions in the AZFc region of the Y chromosome in future generations?

Another patient with an interstitial deletion of chromosome 9: case report and a review of six cases with del(9)(q22q32)

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