Overview
Kathelijn Keymolen practices practicing medicine in Brussels, Belgium.
Keymolen is highly rated in 7 conditions, according to our data. Their clinical expertise encompasses Bone Dysplasia Corpus Callosum Agenesis, Cortical Dysplasia, Focal or Multifocal Malformations in Neuronal Migration, and Trichothiodystrophy.
They are actively involved in clinical research, co-authoring 56 peer reviewed articles.
Locations
Brussels, BRU, Belgium
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Experts who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.
Frequently Asked Questions about Kathelijn Keymolen
Is Kathelijn Keymolen a top-rated expert for Bone Dysplasia Corpus Callosum Agenesis?
MediFind is an objective health platform that identifies experts based on real-world data. Kathelijn Keymolen is classified as an Advanced expert for Bone Dysplasia Corpus Callosum Agenesis, meaning they are among the top experts in the country for this condition. This ranking is based on their volume of patients, published research, and peer connections.
Does Kathelijn Keymolen participate in research or clinical trials?
Yes. Kathelijn Keymolen has published 56 articles and abstracts on conditions like Bone Dysplasia Corpus Callosum Agenesis. You can view a list of Kathelijn Keymolen's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Areas of Expertise
MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.
Learn more about MediFind’s expert tiers
- Advanced
- Achalasia Microcephaly Syndrome
- Bone Dysplasia Corpus Callosum Agenesis
- Cortical DysplasiaKeymolen isAdvanced. Learn about Cortical Dysplasia.
- Focal or Multifocal Malformations in Neuronal Migration
- LissencephalyKeymolen isAdvanced. Learn about Lissencephaly.
- MicrocephalyKeymolen isAdvanced. Learn about Microcephaly.
- TrichothiodystrophyKeymolen isAdvanced. Learn about Trichothiodystrophy.
- Experienced
- Achard SyndromeKeymolen isExperienced. Learn about Achard Syndrome.
- Acromicric DysplasiaKeymolen isExperienced. Learn about Acromicric Dysplasia.
- Aplasia Cutis CongenitaKeymolen isExperienced. Learn about Aplasia Cutis Congenita.
- ArachnodactylyKeymolen isExperienced. Learn about Arachnodactyly.
- Arthrogryposis Multiplex CongenitaKeymolen isExperienced. Learn about Arthrogryposis Multiplex Congenita.
- Autosomal Recessive Primary Microcephaly
- Cerebellar HypoplasiaKeymolen isExperienced. Learn about Cerebellar Hypoplasia.
- Clouston SyndromeKeymolen isExperienced. Learn about Clouston Syndrome.
- Congenital Contractural Arachnodactyly
- Congenital ContracturesKeymolen isExperienced. Learn about Congenital Contractures.
- Corpus Callosum AgenesisKeymolen isExperienced. Learn about Corpus Callosum Agenesis.
- Ectodermal DysplasiasKeymolen isExperienced. Learn about Ectodermal Dysplasias.
- EpilepsyKeymolen isExperienced. Learn about Epilepsy.
- Exocrine Pancreatic InsufficiencyKeymolen isExperienced. Learn about Exocrine Pancreatic Insufficiency.
- Familial Multiple LipomatosisKeymolen isExperienced. Learn about Familial Multiple Lipomatosis.
- Familial PorencephalyKeymolen isExperienced. Learn about Familial Porencephaly.
- Focal Dermal HypoplasiaKeymolen isExperienced. Learn about Focal Dermal Hypoplasia.
- HemangioblastomaKeymolen isExperienced. Learn about Hemangioblastoma.
- HemangiomaKeymolen isExperienced. Learn about Hemangioma.
- Hereditary Hemorrhagic Telangiectasia
- HydrocephalusKeymolen isExperienced. Learn about Hydrocephalus.
- Immune Defect due to Absence of Thymus
- Linear Hamartoma SyndromeKeymolen isExperienced. Learn about Linear Hamartoma Syndrome.
- Marfan SyndromeKeymolen isExperienced. Learn about Marfan Syndrome.
- Microcephalic Osteodysplastic Primordial Dwarfism Type 1 (MOPD1)
- Microcephalic Osteodysplastic Primordial Dwarfism Type 2 (MOPD2)
- MosaicismKeymolen isExperienced. Learn about Mosaicism.
- Multiple Sulfatase DeficiencyKeymolen isExperienced. Learn about Multiple Sulfatase Deficiency.
- Periventricular HeterotopiaKeymolen isExperienced. Learn about Periventricular Heterotopia.
- PolymicrogyriaKeymolen isExperienced. Learn about Polymicrogyria.
- PorencephalyKeymolen isExperienced. Learn about Porencephaly.
- Short Stature (Growth Disorders)Keymolen isExperienced. Learn about Short Stature (Growth Disorders).
- Shwachman-Diamond SyndromeKeymolen isExperienced. Learn about Shwachman-Diamond Syndrome.
- Spinal Muscular Atrophy Type 2Keymolen isExperienced. Learn about Spinal Muscular Atrophy Type 2.
- Spinal Muscular Atrophy Type 3Keymolen isExperienced. Learn about Spinal Muscular Atrophy Type 3.
- Spinal Muscular Atrophy with Arthrogryposis
- Tomaculous NeuropathyKeymolen isExperienced. Learn about Tomaculous Neuropathy.
- Tuberous SclerosisKeymolen isExperienced. Learn about Tuberous Sclerosis.
- Tuberous Sclerosis ComplexKeymolen isExperienced. Learn about Tuberous Sclerosis Complex.
- Vein of Galen AneurysmKeymolen isExperienced. Learn about Vein of Galen Aneurysm.
- Von Hippel-Lindau (VHL) SyndromeKeymolen isExperienced. Learn about Von Hippel-Lindau (VHL) Syndrome.
- X-Linked IchthyosisKeymolen isExperienced. Learn about X-Linked Ichthyosis.
- Xeroderma PigmentosumKeymolen isExperienced. Learn about Xeroderma Pigmentosum.