Overview
Nicola Brunetti-Pierri is a Pediatrics specialist and a Medical Genetics provider practicing medicine in Houston, Texas.
Dr. Brunetti-Pierri is highly rated in 40 conditions, according to our data. His clinical expertise encompasses Pyruvate Decarboxylase Deficiency, Crigler-Najjar Syndrome, Argininosuccinic Aciduria, and Rotor Syndrome.
He is actively involved in clinical research, co-authoring 217 peer reviewed articles.
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Locations
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Providers 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.
Texas Childrens Physician Group
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Lorraine Potocki is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Houston, Texas. Dr. Potocki is highly rated in 10 conditions, according to our data. Her clinical expertise encompasses Potocki-Lupski Syndrome, Smith-Magenis Syndrome, Hypotonia, and Trisomy 17 Mosaicism. Dr. Potocki is currently accepting new patients.
Baylor College Of Medicine
Fernando Scaglia is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Houston, Texas. Dr. Scaglia is highly rated in 22 conditions, according to our data. His clinical expertise encompasses MELAS Syndrome, Hypotonia, Primary Carnitine Deficiency, and Leigh Syndrome. Dr. Scaglia is currently accepting new patients.
Frequently Asked Questions about Dr. Nicola Brunetti-Pierri
How do I make an appointment with Dr. Nicola Brunetti-Pierri?
You can book an appointment with Dr. Nicola Brunetti-Pierri by calling their office at 713-798-1750. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Nicola Brunetti-Pierri a top-rated expert for Pyruvate Decarboxylase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Nicola Brunetti-Pierri is classified as an Elite expert for Pyruvate Decarboxylase Deficiency, 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.
What conditions does Dr. Nicola Brunetti-Pierri specialize in?
While Dr. Nicola Brunetti-Pierri is a Pediatrics, they have specific expertise in Pyruvate Decarboxylase Deficiency, Crigler-Najjar Syndrome, and Argininosuccinic Aciduria. MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Pediatrics.
Does Dr. Nicola Brunetti-Pierri participate in research or clinical trials?
Yes. Dr. Nicola Brunetti-Pierri has published 210 articles and abstracts on conditions like Pyruvate Decarboxylase Deficiency. You can view a list of Dr. Nicola Brunetti-Pierri'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
- Elite
- Argininosuccinic AciduriaDr. Brunetti-Pierri isElite. Learn about Argininosuccinic Aciduria.
- Crigler-Najjar SyndromeDr. Brunetti-Pierri isElite. Learn about Crigler-Najjar Syndrome.
- Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome)
- Myhre SyndromeDr. Brunetti-Pierri isElite. Learn about Myhre Syndrome.
- Pyruvate Decarboxylase DeficiencyDr. Brunetti-Pierri isElite. Learn about Pyruvate Decarboxylase Deficiency.
- Pyruvate Dehydrogenase DeficiencyDr. Brunetti-Pierri isElite. Learn about Pyruvate Dehydrogenase Deficiency.
- Distinguished
- Achalasia Microcephaly SyndromeDr. Brunetti-Pierri isDistinguished. Learn about Achalasia Microcephaly Syndrome.
- Allan-Herndon-Dudley SyndromeDr. Brunetti-Pierri isDistinguished. Learn about Allan-Herndon-Dudley Syndrome.
- Atresia of Small IntestineDr. Brunetti-Pierri isDistinguished. Learn about Atresia of Small Intestine.
- Carbamoyl Phosphate Synthetase 1 DeficiencyDr. Brunetti-Pierri isDistinguished. Learn about Carbamoyl Phosphate Synthetase 1 Deficiency.
- Cortical DysplasiaDr. Brunetti-Pierri isDistinguished. Learn about Cortical Dysplasia.
- HypotoniaDr. Brunetti-Pierri isDistinguished. Learn about Hypotonia.
- Advanced
- Acromicric DysplasiaDr. Brunetti-Pierri isAdvanced. Learn about Acromicric Dysplasia.
- Alpha-1 Antitrypsin Deficiency (AATD)Dr. Brunetti-Pierri isAdvanced. Learn about Alpha-1 Antitrypsin Deficiency (AATD).
- Autism Spectrum DisorderDr. Brunetti-Pierri isAdvanced. Learn about Autism Spectrum Disorder.
- Bardet-Biedl SyndromeDr. Brunetti-Pierri isAdvanced. Learn about Bardet-Biedl Syndrome.
- Bilateral Perisylvian PolymicrogyriaDr. Brunetti-Pierri isAdvanced. Learn about Bilateral Perisylvian Polymicrogyria.
- BlepharophimosisDr. Brunetti-Pierri isAdvanced. Learn about Blepharophimosis.
- Experienced
- Aplasia Cutis CongenitaDr. Brunetti-Pierri isExperienced. Learn about Aplasia Cutis Congenita.
- Arthrogryposis Multiplex CongenitaDr. Brunetti-Pierri isExperienced. Learn about Arthrogryposis Multiplex Congenita.
- Brachydactyly Mononen TypeDr. Brunetti-Pierri isExperienced. Learn about Brachydactyly Mononen Type.
- C SyndromeDr. Brunetti-Pierri isExperienced. Learn about C Syndrome.
- Cat Eye SyndromeDr. Brunetti-Pierri isExperienced. Learn about Cat Eye Syndrome.
- Clouston SyndromeDr. Brunetti-Pierri isExperienced. Learn about Clouston Syndrome.