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Severe cortical malformation and acquired cataract – An unusual presentation of DYNC1H1 mutation in twins

European journal of paediatric neurology, 2017-06, Vol.21, p.e75-e76

2017

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Prediction of ROP Treatment and Evaluation of Screening Criteria in VLBW Infants–a Population Based Analysis

Pediatric research, 2018-11, Vol.84 (5), p.632-638

2018

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Intrauterine subdural hemorrhage in a preterm neonate possibly associated with maternal low-molecular weight heparin treatment

Journal of perinatology, 2009-07, Vol.29 (7), p.521-523

2009

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Incidence of retinopathy of prematurity (ROP) and ROP treatment in Switzerland 2006–2015: a population-based analysis

Archives of disease in childhood. Fetal and neonatal edition, 2018-07, Vol.103 (4), p.F337-F342

2018

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PHO05 Recessive hyperekplexia in three Turkish patients

European journal of paediatric neurology, 2007, Vol.11, p.32-33

2007

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Severe Cortical Malformation and Acquired Cataract: An Unusual Presentation of DYNC1H1 Mutation in Twins

Neuropediatrics, 2017, Vol.48 (S 01), p.S1-S45

2017

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Short-term neurological improvement in neonates with hypoxic-ischemic encephalopathy predicts neurodevelopmental outcome at 18-24 months

Journal of perinatal medicine, 2020-03, Vol.48 (3), p.296-303

2020

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Two Cases of an Unusual Cause of Headache and Papilledema not to be Missed

Neuropediatrics, 2016, Vol.47 (S 01)

2016

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Outcome of extremely low gestational age newborns (ELGANs) following a pro-active treatment approach: a Swiss single centre experience over 10 years

Swiss medical weekly, 2014-01, Vol.144, p.w14014

2014

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Association between perinatal interventional activity and 2-year outcome of Swiss extremely preterm born infants: a population-based cohort study

BMJ open, 2019-03, Vol.9 (3), p.e024560-e024560

2019

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Neurodevelopmental outcome at early school age in a Swiss national cohort of very preterm children

Swiss medical weekly, 2019-06, Vol.149, p.w20084

2019

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Primary central nervous system vasculitis in childhood: more frequent and variable than thought

Neuropediatrics, 2013, Vol.44 (2)

2013

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Activated protein C (APC) resistance: does it exist in Basques?

British journal of haematology, 1997-12, Vol.99 (3), p.712-713

1997

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Neonatal seizures: eyes open or closed?

Neuropediatrics, 2006, Vol.37 (3)

2006

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Double peripheral blood stem cell autograft for multiple myeloma. Experience of Centre François Baclesse of 4 patients

Bone marrow transplantation (Basingstoke), 1990, Vol.5, p.79-80

1990

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CYSTIC PERIVENTRICULAR LEUKOMALACIA (PVL): INCIDENCE AND ASSOCIATED FACTORS IN SWITZERLAND 1995-1997

Pediatric research, 1999-06, Vol.45 (6), p.921-921

1999

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Sonographisch nachgewiesene zystische periventrikuläre Leukomalazie (PVL): Inzidenz und assoziierte Faktoren in der Schweiz 1995 - 1997

Zeitschrift für Geburtshilfe und Neonatologie, 2000-04, Vol.204 (2), p.68-73

2000

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Ultrasonically established cystic periventricular leukomalacia (PVL): incidence and associated factors in Switzerland 1995-1997

Zeitschrift für Geburtshilfe und Neonatologie, 2000-03, Vol.204 (2), p.68

2000

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Familial mental retardation in a family with an inherited chromosome rearrangement

Journal of medical genetics, 1974-12, Vol.11 (4), p.353-366

1974

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A contactless transfer device for power and data

1996 IEEE Aerospace Applications Conference. Proceedings, 1996, Vol.2, p.333-345 vol.2

1996

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Deletion of the short arm of chromosome No. 10

Journal of medical genetics, 1975-03, Vol.12 (1), p.99-103

1975

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Exclusion of Peptidase-A Structural Gene Locus from the q11q21 Region of Chromosome 18 in Man

Cytogenetic and genome research, 1974-01, Vol.13 (1-2), p.126-127

1974

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Quality of light

Journal of the Franklin Institute, 1910-01, Vol.169 (3), p.223-237

Bauder, Paul F.

1910

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Design and evaluation of the power and data contactless transfer device

1997 IEEE Aerospace Conference, 1997, Vol.3, p.523-533 vol.3

1997

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Down and Turner syndromes in a female infant with 47,X,del(X)(p11),+21

Human genetics, 1977-01, Vol.39 (1), p.103-108

1977

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Severe cortical malformation and acquired cataract – An unusual presentation of DYNC1H1 mutation in twins

Prediction of ROP Treatment and Evaluation of Screening Criteria in VLBW Infants–a Population Based Analysis

Intrauterine subdural hemorrhage in a preterm neonate possibly associated with maternal low-molecular weight heparin treatment

Incidence of retinopathy of prematurity (ROP) and ROP treatment in Switzerland 2006–2015: a population-based analysis

PHO05 Recessive hyperekplexia in three Turkish patients

Severe Cortical Malformation and Acquired Cataract: An Unusual Presentation of DYNC1H1 Mutation in Twins

Short-term neurological improvement in neonates with hypoxic-ischemic encephalopathy predicts neurodevelopmental outcome at 18-24 months

Two Cases of an Unusual Cause of Headache and Papilledema not to be Missed

Outcome of extremely low gestational age newborns (ELGANs) following a pro-active treatment approach: a Swiss single centre experience over 10 years

Association between perinatal interventional activity and 2-year outcome of Swiss extremely preterm born infants: a population-based cohort study

Neurodevelopmental outcome at early school age in a Swiss national cohort of very preterm children

Primary central nervous system vasculitis in childhood: more frequent and variable than thought

Activated protein C (APC) resistance: does it exist in Basques?

Neonatal seizures: eyes open or closed?

Double peripheral blood stem cell autograft for multiple myeloma. Experience of Centre François Baclesse of 4 patients

CYSTIC PERIVENTRICULAR LEUKOMALACIA (PVL): INCIDENCE AND ASSOCIATED FACTORS IN SWITZERLAND 1995-1997

Sonographisch nachgewiesene zystische periventrikuläre Leukomalazie (PVL): Inzidenz und assoziierte Faktoren in der Schweiz 1995 - 1997

Ultrasonically established cystic periventricular leukomalacia (PVL): incidence and associated factors in Switzerland 1995-1997

Familial mental retardation in a family with an inherited chromosome rearrangement

A contactless transfer device for power and data

Deletion of the short arm of chromosome No. 10

Exclusion of Peptidase-A Structural Gene Locus from the q11q21 Region of Chromosome 18 in Man

Quality of light

Design and evaluation of the power and data contactless transfer device

Down and Turner syndromes in a female infant with 47,X,del(X)(p11),+21

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