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Phelan-mcdermid Syndrome in an Adult Female with Mild Intellectual Disability

European psychiatry, 2015-03, Vol.30, p.863-863

2015

Volltextzugriff (PDF)

The Clinical Spectrum of General Paralysis of the Insane: a Historical Cohort Study

European psychiatry, 2015-03, Vol.30, p.1247-1247

2015

Volltextzugriff (PDF)

P-711 - Genetic syndromes and the autism spectrum

European psychiatry, 2012, Vol.27, p.1-1

2012

Volltextzugriff (PDF)

536 – Acute intermittent porphyria and cycloid psychosis

European psychiatry, 2013, Vol.28, p.1-1

2013

Volltextzugriff (PDF)

535 – The clinical spectrum of neurosyphilis today

European psychiatry, 2013, Vol.28, p.1-1

2013

Volltextzugriff (PDF)

P-713 - A de novo microdeletion in chromosome 8q12.3q13.2: association with mild intellectual disability and epilepsy?

European psychiatry, 2012, Vol.27, p.1-1

2012

Volltextzugriff (PDF)

P02-223 - Kleefstra syndrome: neuropsychiatric sequelae

European psychiatry, 2011, Vol.26, p.819-819

2011

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P-700 - Social cognition and the behavioural phenotype of 17q21.31 microdeletion syndrome

European psychiatry, 2012, Vol.27, p.1-1

2012

Volltextzugriff (PDF)

P-701 - Executive dysfunctions as part of the behavioural phenotype of aarskog-scott syndrome

European psychiatry, 2012, Vol.27, p.1-1

2012

Volltextzugriff (PDF)

P-712 - Polg mutation in a patient with recurrent major depression, cardiomyopathy and ataxia

European psychiatry, 2012, Vol.27, p.1-1

2012

Volltextzugriff (PDF)

P-449 - Prognostic factors regarding the treatment of dementia paralytica with malaria fever therapy: a historical cohort study

European psychiatry, 2012, Vol.27, p.1-1

2012

Volltextzugriff (PDF)

W01-03 - Neuropsychological phenotyping of genetic syndromes

European psychiatry, 2012, Vol.27, p.1-1

2012

Volltextzugriff (PDF)

P02-224 - Behavioural phenotype of noonan syndrome in adulthood

European psychiatry, 2011, Vol.26, p.820-820

2011

Volltextzugriff (PDF)

W04-03 - Prevalence of catatonia in psychoses

European psychiatry, 2010, Vol.25 (S1), p.144-144, Article 25-E144

2010

Volltextzugriff (PDF)

P-1064 - Cycloid psychoses: Leonhard's descriptions revisited

European psychiatry, 2012, Vol.27, p.1-1

2012

Volltextzugriff (PDF)

P02-222 - Clinical phenomena of Charlevoix-Saguenay ataxia in two adult brothers

European psychiatry, 2011, Vol.26, p.818-818

2011

Volltextzugriff (PDF)

P03-353 - Neurotrophic proteins and symptom profile in psychotic disorders

European psychiatry, 2011, Vol.26, p.1523-1523

2011

Volltextzugriff (PDF)

Psychiatric Profile in Rubinstein-Taybi Syndrome

Psychopathology, 2009-12, Vol.43 (1), p.63-68

2009

Volltextzugriff (PDF)

P03-46 - Fluid intelligence and executive functioning: Partial overlap in patients with psychiatric disorders

European psychiatry, 2011, Vol.26, p.1215-1215

2011

Volltextzugriff (PDF)

Differentiated psychopharmacological treatment in three genetic subtypes of 22q11.2 deletion syndrome

European psychiatry, 2017-04, Vol.41 (S1), p.S388-S389

2017

Volltextzugriff (PDF)

P.3.c.012 Metabolic syndrome among patients with psychotic disorders treated with clozapine

European neuropsychopharmacology, 2008, Vol.18, p.S411-S411

2008

Volltextzugriff (PDF)

P.2.b.001 Treatment with electroconvulsive therapy is associated with an increase of nitric oxide synthesis

European neuropsychopharmacology, 2007, Vol.17, p.S332-S333

2007

Volltextzugriff (PDF)

Kleefstra syndrome: Considerations about treatment strategy in 2 patients with a causative Ehmt1 mutation and apathy

European psychiatry, 2017-04, Vol.41 (S1), p.S600-S600

2017

Volltextzugriff (PDF)

P.1.g.001 Hypothalamic hamartoma and psychiatry

European neuropsychopharmacology, 2007, Vol.17, p.S302-S303

2007

Volltextzugriff (PDF)

P.1.g.002 Psychopathology and social cognition in 10 patients with Noonan syndrome

European neuropsychopharmacology, 2007, Vol.17, p.S303-S303

2007

Volltextzugriff (PDF)

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Phelan-mcdermid Syndrome in an Adult Female with Mild Intellectual Disability

The Clinical Spectrum of General Paralysis of the Insane: a Historical Cohort Study

P-711 - Genetic syndromes and the autism spectrum

536 – Acute intermittent porphyria and cycloid psychosis

535 – The clinical spectrum of neurosyphilis today

P-713 - A de novo microdeletion in chromosome 8q12.3q13.2: association with mild intellectual disability and epilepsy?

P02-223 - Kleefstra syndrome: neuropsychiatric sequelae

P-700 - Social cognition and the behavioural phenotype of 17q21.31 microdeletion syndrome

P-701 - Executive dysfunctions as part of the behavioural phenotype of aarskog-scott syndrome

P-712 - Polg mutation in a patient with recurrent major depression, cardiomyopathy and ataxia

P-449 - Prognostic factors regarding the treatment of dementia paralytica with malaria fever therapy: a historical cohort study

W01-03 - Neuropsychological phenotyping of genetic syndromes

P02-224 - Behavioural phenotype of noonan syndrome in adulthood

W04-03 - Prevalence of catatonia in psychoses

P-1064 - Cycloid psychoses: Leonhard's descriptions revisited

P02-222 - Clinical phenomena of Charlevoix-Saguenay ataxia in two adult brothers

P03-353 - Neurotrophic proteins and symptom profile in psychotic disorders

Psychiatric Profile in Rubinstein-Taybi Syndrome

P03-46 - Fluid intelligence and executive functioning: Partial overlap in patients with psychiatric disorders

Differentiated psychopharmacological treatment in three genetic subtypes of 22q11.2 deletion syndrome

P.3.c.012 Metabolic syndrome among patients with psychotic disorders treated with clozapine

P.2.b.001 Treatment with electroconvulsive therapy is associated with an increase of nitric oxide synthesis

Kleefstra syndrome: Considerations about treatment strategy in 2 patients with a causative Ehmt1 mutation and apathy

P.1.g.001 Hypothalamic hamartoma and psychiatry

P.1.g.002 Psychopathology and social cognition in 10 patients with Noonan syndrome

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