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Advanced endoscopic techniques used in dysfunctional bleeding, fibroids and endometriosis, and the role of gonadotrophin‐releasing hormone agonist treatment

BJOG : an international journal of obstetrics and gynaecology, 1994-05, Vol.101 (s10), p.2-9

1994

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The place of GnRH agonists in the treatment of endometriosis and fibroids by advanced endoscopic techniques

BJOG : an international journal of obstetrics and gynaecology, 1992-02, Vol.99 (s7), p.31-33

1992

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Mutations in FKBP10 cause recessive osteogenesis imperfecta and bruck syndrome

Journal of bone and mineral research, 2011-03, Vol.26 (3), p.666-672

2011

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Growth resistance and resilience of mixed silver fir and Norway spruce forests in central Europe: Contrasting responses to mild and severe droughts

Global change biology, 2021-09, Vol.27 (18), p.4403-4419

2021

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Forest structure and composition alleviate human thermal stress

Global change biology, 2022-12, Vol.28 (24), p.7340-7352

2022

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Forest canopies as nature‐based solutions to mitigate global change effects on people and nature

The Journal of ecology, 2024-05

2024

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Prenatal diagnosis of severe structural congenital malformations in Europe

Ultrasound in obstetrics & gynecology, 2005-01, Vol.25 (1), p.6-11

2005

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Coenzyme Q- responsive Leigh's encephalopathy in two sisters

Annals of neurology, 2002-12, Vol.52 (6), p.750-754

2002

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Survey of prenatal screening policies in Europe for structural malformations and chromosome anomalies, and their impact on detection and termination rates for neural tube defects and Down’s syndrome

BJOG : an international journal of obstetrics and gynaecology, 2008-05, Vol.115 (6), p.689-696

2008

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Associated anomalies in multi-malformed infants with cleft lip and palate: An epidemiologic study of nearly 6 million births in 23 EUROCAT registries

American journal of medical genetics. Part A, 2007-03, Vol.143A (6), p.528-537

2007

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Blepharophimosis-mental retardation (BMR) syndromes: A proposed clinical classification of the so-called Ohdo syndrome, and delineation of two new BMR syndromes, one X-linked and one autosomal recessive

American journal of medical genetics. Part A, 2006-06, Vol.140A (12), p.1285-1296

2006

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Recto vaginal septum adenomyotic nodules: a series of 500 cases

BJOG : an international journal of obstetrics and gynaecology, 1997-09, Vol.104 (9), p.1014-1018

1997

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Descriptive epidemiology of Cornelia de Lange syndrome in Europe

American journal of medical genetics. Part A, 2008-01, Vol.146A (1), p.51-59

2008

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Isolated bilateral transverse agenesis of the distal segments of the lower limbs at the level of the knee joint in a human fetus

American journal of medical genetics. Part A, 2016-02, Vol.170A (2), p.523-530

2016

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Prenatal diagnostic procedures used in pregnancies with congenital malformations in 14 regions of Europe

Prenatal diagnosis, 2004-11, Vol.24 (11), p.908-912

2004

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Prenatal diagnosis of trisomy 6 mosaicism

Prenatal diagnosis, 2005-05, Vol.25 (5), p.354-357

2005

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A rare case of de novo distal 19q trisomy prenatally diagnosed

Prenatal diagnosis, 2004-10, Vol.24 (10), p.822-827

2004

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Prenatal diagnosis of six major cardiac malformations in Europe - A population based study

Acta obstetricia et gynecologica Scandinavica, 2001-03, Vol.80 (3), p.224-228

Garne, Ester

2001

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Oro-facial-digital syndrome II

Clinical genetics, 1988-02, Vol.33 (2), p.141-142

1988

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Morphological features of a case of retinoic acid embryopathy

Prenatal diagnosis, 1992-08, Vol.12 (8), p.699-701

1992

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Vasopressin and gonadotropin deficiency in a boy with the ectrodactyly‐ectodermal dysplasia‐clefting syndrome

Acta Paediatrica, 1992-04, Vol.81 (4), p.365-367

1992

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Variability versus heterogeneity in syndromal hypothalamic hamartoblastoma and related disorders: Review and delineation of the Cerebro-Acro-Visceral Early lethality (CAVE) multiplex syndrome

American journal of medical genetics, 1992-07, Vol.43 (4), p.669-677

1992

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Mental retardation with blepharo-naso-facial abnormalities and hand malformations: a new syndrome?

Clinical genetics, 1992-01, Vol.41 (1), p.22-24

1992

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Primordial osteodysplastic dwarfism type I in association with corneal clouding: evidence for autosomal recessive inheritance

Clinical genetics, 1990-11, Vol.38 (5), p.359-361

1990

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Neural tube defects and omphalocele in trisomy 18

Clinical genetics, 1989-01, Vol.35 (1), p.77-78

1989

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Advanced endoscopic techniques used in dysfunctional bleeding, fibroids and endometriosis, and the role of gonadotrophin‐releasing hormone agonist treatment

The place of GnRH agonists in the treatment of endometriosis and fibroids by advanced endoscopic techniques

Mutations in FKBP10 cause recessive osteogenesis imperfecta and bruck syndrome

Growth resistance and resilience of mixed silver fir and Norway spruce forests in central Europe: Contrasting responses to mild and severe droughts

Forest structure and composition alleviate human thermal stress

Forest canopies as nature‐based solutions to mitigate global change effects on people and nature

Prenatal diagnosis of severe structural congenital malformations in Europe

Coenzyme Q- responsive Leigh's encephalopathy in two sisters

Survey of prenatal screening policies in Europe for structural malformations and chromosome anomalies, and their impact on detection and termination rates for neural tube defects and Down’s syndrome

Associated anomalies in multi-malformed infants with cleft lip and palate: An epidemiologic study of nearly 6 million births in 23 EUROCAT registries

Blepharophimosis-mental retardation (BMR) syndromes: A proposed clinical classification of the so-called Ohdo syndrome, and delineation of two new BMR syndromes, one X-linked and one autosomal recessive

Recto vaginal septum adenomyotic nodules: a series of 500 cases

Descriptive epidemiology of Cornelia de Lange syndrome in Europe

Isolated bilateral transverse agenesis of the distal segments of the lower limbs at the level of the knee joint in a human fetus

Prenatal diagnostic procedures used in pregnancies with congenital malformations in 14 regions of Europe

Prenatal diagnosis of trisomy 6 mosaicism

A rare case of de novo distal 19q trisomy prenatally diagnosed

Prenatal diagnosis of six major cardiac malformations in Europe - A population based study

Oro-facial-digital syndrome II

Morphological features of a case of retinoic acid embryopathy

Vasopressin and gonadotropin deficiency in a boy with the ectrodactyly‐ectodermal dysplasia‐clefting syndrome

Variability versus heterogeneity in syndromal hypothalamic hamartoblastoma and related disorders: Review and delineation of the Cerebro-Acro-Visceral Early lethality (CAVE) multiplex syndrome

Mental retardation with blepharo-naso-facial abnormalities and hand malformations: a new syndrome?

Primordial osteodysplastic dwarfism type I in association with corneal clouding: evidence for autosomal recessive inheritance

Neural tube defects and omphalocele in trisomy 18

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