Dr. Bertil Glader, MD
Palo Alto, CA
51 Years of Experience
Affiliated with a Castle Connolly Top Hospital
Who is Dr. Glader, Pediatric Hematologist-Oncologist in Palo Alto, CA?
Dr. Bertil Glader, MD is a Pediatric Hematologist-Oncologist, who primarily practices in Palo Alto, CA. He has been practicing for over 51 years and is board certified by the American Board of Pediatrics. Dr. Glader graduated from Northwestern University The Feinberg School of Medicine and completed his residency at Children'S Hosp, Internal Medicine; Stanford Univ Hosp, Pediatrics. Dr. Glader is fluent in English and Spanish, and is currently seeing new patients. Dr. Glader’s practice accepts Kaiser Permanente, Medicare, UnitedHealthcare, Aetna, Cigna and other major insurance plans. To book an appointment or to confirm insurance options, please call Dr. Glader’s office at (650) 497-8000.
What are Areas of Expertise for Dr. Glader?
Dr. Bertil Glader, MD is a highly-rated, board-certified Pediatric Hematologist-Oncologist known for expertly diagnosing, treating, and managing a wide array of related conditions or procedures. Utilizing the latest medical advancements and evidence-based practices, Dr. Glader empowers patients to confidently navigate their health journey, specializing in Genetic Disorders-Blood, Hemophilia, or comprehensive wellness support. Serving the Palo Alto/CA community, Dr. Glader is dedicated to enhancing lives through expert, patient-centered care.
Where did Dr. Glader go to medical school and complete their residency?
Residency: Children'S Hosp, Internal Medicine; Stanford Univ Hosp, Pediatrics | Chldns Hospital Med Center | Children's Hospital Program
Medical School: Northwestern Uniiversity | Northwestern University The Feinberg School of Medicine
Is Dr. Glader board certified in Pediatric Hematologist-Oncologist?
Yes, Dr. Bertil Glader, MD is board certified by the American Board of Pediatrics
What languages does Dr. Glader speak?
Dr. Glader and their clinical team can communicate with patients in the following languages:
English
Spanish
What conditions does Dr. Glader treat?
As a Pediatric Hematologist-Oncologist, Dr. Glader diagnoses, treats, and manages a wide range of conditions. This condition information is derived from anonymized insurance claims and highlights the medical conditions most commonly treated by Dr. Glader. It provides insight into the doctor’s areas of experience and expertise based on real-world patient encounters from the past two years, updated quarterly.
Also known as:
- Hereditary Spherocytosis
- Iron Deficiency Anemia
- Anemia
- Iron Deficiency Anemia from Chronic Blood Loss
- Hereditary spherocytosis
- Iron
- Congenital Hemolytic Anemia
- Minkowski-Chauffard Disease
- Anemia from Iron Lack
- Low Iron Anemia
- Sideropenic Anemia
- Low Red Blood Cell Count
- Low Hemoglobin
- Iron deficiency
- Anemia due to iron deficiency and blood loss
- Chronic blood loss anemia
- Low iron anemia from bleeding
ICD-10 Codes:
- D580: Hereditary spherocytosis
- D509: Iron deficiency anemia, unspecified
- D508: Other iron deficiency anemias
- D649: Anemia, unspecified
- D500: Iron deficiency anemia secondary to blood loss (chronic)
Also known as:
- Aplastic Anemia
- Diamond-Blackfan Anemia
- Anemia
- Diamond-Blackfan anemia
- Bone Marrow Failure Anemia
- Marrow Aplasia
- DBA
- Congenital pure red cell aplasia
- Inherited red cell aplasia
ICD-10 Codes:
- D619: Aplastic anemia, unspecified
- D6101: Constitutional (pure) red blood cell aplasia
Also known as:
- Beta Thalassemia
- Alpha Thalassemia
- Hemoglobin E-Beta Thalassemia
- Thalassemia
- Beta thalassemia
- Alpha thalassemia
- Alpha thalassemia X-linked intellectual disability syndrome
- Beta-thalassemia major', 'Cooley's anemia
- Thalassemia intermedia
- Alpha Thalassemia Trait
- Hemoglobin H Disease
- Hb E-Beta Thalassemia
- Hemoglobin E Thalassemia
ICD-10 Codes:
- D561: Beta thalassemia
- D560: Alpha thalassemia
- D565: Hemoglobin E-beta thalassemia
Also known as:
- Immune Thrombocytopenic Purpura
- Thrombocytopenia
- Platelet Disorder
- Immune thrombocytopenia
- ITP
- Idiopathic thrombocytopenic purpura
- Low platelet count
- Platelet deficiency
- Bleeding disorder
ICD-10 Codes:
- D693: Immune thrombocytopenic purpura
- D696: Thrombocytopenia, unspecified
Also known as:
- Hemophilia A
- Hemophilia
- Factor VIII Deficiency', 'Classic Hemophilia', 'Bleeder's Disease
ICD-10 Codes:
- D66: Hereditary factor VIII deficiency
Also known as:
- Paroxysmal Nocturnal Hemoglobinuria
- Other Hemoglobin Disorder
- Anemia
- Urine and Urination
- Paroxysmal nocturnal hemoglobinuria
- PNH
- Marchiafava-Micheli syndrome
- Dark urine anemia
- Rare hemoglobinopathy
- Uncommon blood disorder
- Genetic blood condition
ICD-10 Codes:
- D595: Paroxysmal nocturnal hemoglobinuria [Marchiafava-Micheli]
- D582: Other hemoglobinopathies
Also known as:
- Other Types of Pancytopenia
- Blood Disorder
- Rare pancytopenia
- Uncommon low blood counts
- Bone marrow failure
ICD-10 Codes:
- D61818: Other pancytopenia
Also known as:
- Low Neutrophil Count
- Blood Disorder
- Neutropenia
- Low white blood cell count
- Neutrophil deficiency
ICD-10 Codes:
- D709: Neutropenia, unspecified
Also known as:
- Evans Syndrome
- Platelet Disorder
- Autoimmune hemolytic anemia and ITP
- Combined autoimmune cytopenias
- Rare autoimmune disorder
ICD-10 Codes:
- D6941: Evans syndrome
Also known as:
- Iron Deficiency
- Iron
- Malnutrition
- Lack of Iron
- Low Iron Levels
- Iron Depletion
ICD-10 Codes:
- E611: Iron deficiency
Also known as:
- G6PD Deficiency
- Glucose-6-phosphate dehydrogenase deficiency
- Favism (in some cases)
- G6PD defect
ICD-10 Codes:
- D75A: Glucose-6-phosphate dehydrogenase (G6PD) deficiency without anemia
Which procedures does Dr. Glader perform as a Pediatric Hematologist-Oncologist?
As a Pediatric Hematologist-Oncologist, procedures performed by a Dr. Bertil Glader may include:
- 3D Conformal Radiotherapy
- Adaptive Radiation Therapy (ART)
- Adrenalectomy
- Blood Thinning Therapy / Anticoagulation
- Blood Transfusion Consultation
- Blood Transfusion Follow Up
- Bone Excision
- Bone Grafting
For detailed information, please contact Dr. Glader's office.
Does Dr. Glader accept my insurance?
Dr. Glader accepts most major insurance plans. Important: Please call our office at (650) 497-8000 before your appointment to verify that your specific plan and network are accepted.
What insurance plans does Dr. Glader accept in Palo Alto, CA?
Dr. Glader in Palo Alto, CA accepts plans from many carriers. While this list is updated regularly, it is not a guarantee of coverage.
Top Insurances
All Other Third Party
Blue Shield of California
California Water Service Group
Central California Alliance for Health
CVS Health (formerly Aetna)
Health Plan of San Mateo
OptumRx
State of California
UnitedHealthcare
Valley Health Plan
View All Insurances
Where is Dr. Glader's office located?
Recognitions
Publications
Novel deletion of RPL15 identified by array-comparative genomic hybridization in Diamond
HUMAN GENETICS, 2013
Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1
BLOOD, 2013
Frameshift mutation in p53 regulator RPL26 is associated with multiple physical abnormalities
HUMAN MUTATION, 2012
Adenovirus-Associated Virus Vector-Mediated Gene Transfer in Hemophilia B
NEW ENGLAND JOURL OF MEDICINE, 2011
Reduced ribosomal protein gene dosage and p53 activation in low-risk myelodysplastic syndrome
BLOOD, 2011
Functiol characterization
AMERICAN JOURL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2011
Development of Antibodies to Human Thrombin
PEDIATRIC BLOOD & CANCER, 2010
Adrel and rel corticomedullary junction iron deposition in red cell aplasia
PEDIATRIC RADIOLOGY, 2010
Ribosomal Protein Genes RPS10 and RPS26 Are Commonly Mutated in Diamond-Blackfan Anemia
AMERICAN JOURL OF HUMAN GENETICS, 2010
Monthly recombint tissue plasminogen activator administration to implantable central venous
HAEMOPHILIA, 2009
One Year Follow-Up of Children and Adolescents With Chronic Immune Thrombocytopenic Purpura
PEDIATRIC BLOOD & CANCER, 2009
Ribosomal Protein L5 and L11 Mutations Are Associated with Cleft Palate and Abnormal Thumbs
AMERICAN JOURL OF HUMAN GENETICS, 2008
Diagnosing and treating Diamond Blackfan aemia
BRITISH JOURL OF HAEMATOLOGY, 2008
Cold agglutinin syndrome in pediatric liver transplant recipients
PEDIATRIC TRANSPLANTATION, 2007
Ribosomal protein S24 gene is mutated in diamond-blackfan anemia
AMERICAN JOURL OF HUMAN GENETICS, 2006
Prospective phase 1/2 study of rituximab in childhood and adolescent chronic immune
BLOOD, 2006
Successful transduction of liver in hemophilia by AAV-factor IX
TURE MEDICINE, 2006
AAV-mediated factor IX gene transfer to skeletal muscle in patients with severe hemophilia B
BLOOD, 2003
Approach to the bleeding child
PEDIATRIC CLINICS OF NORTH AMERICA, 2002
Resolution of severe Doth-L
CRITICAL CARE MEDICINE, 2002
Bilateral microtia and cleft palate in cousins with Diamond-Blackfan anemia
AMERICAN JOURL OF MEDICAL GENETICS, 2001
Evidence for linkage of familial Diamond-Blackfan anemia to chromosome 8p23.3-p22
BLOOD, 2001
Evidence for gene transfer
TURE GENETICS, 2000
Hemolytic anemia in children
CLINICS IN LABORATORY MEDICINE, 1999
Home treatment of mild to moderate bleeding episodes using recombint factor VIIa
THROMBOSIS AND HAEMOSTASIS, 1998
Bone marrow transplant in thalassemia - A role for radiation?
COOLEYS ANEMIA, 1998
Acute idiopathic thrombocytopenic purpura - Magement in childhood
BLOOD, 1997
Loss of elbow and wrist motion in hemophilia
CLINICAL ORTHOPAEDICS AND RELATED RESEARCH, 1996
Hematologic disorders in children from Southeast Asia
PEDIATRIC CLINICS OF NORTH AMERICA, 1996
FREQUENCY OF INHIBITOR DEVELOPMENT IN HEMOPHILIACS TREATED WITH LOW-PURITY FACTOR-VIII
LANCET, 1993
LANGERHANS CELL HISTIOCYTOSIS PRESENTING WITH THE SUPERIOR VE-CAVA SYNDROME - A CASE-REPORT
MEDICAL AND PEDIATRIC ONCOLOGY, 1993
Arthropathy of the ankle in hemophilia.
jourl of bone and joint surgery. American volume, 1991
CRYPTOCOCCUS INFECTION IN A 9-YEAR
PEDIATRIC INFECTIOUS DISEASE JOURL, 1991
TREATMENT OF NEUTROPENIA ASSOCIATED WITH DYSKERATOSIS CONGENITA WITH GRANULOCYTE-MACROPHAGE COLONY
LANCET, 1990
RED-BLOOD-CELL APLASIAS IN CHILDREN
PEDIATRIC ANLS, 1990
CONGENITAL HYPOPLASTIC (DIAMOND-BLACKFAN) ANEMIA IN 7 MEMBERS OF ONE KINDRED
AMERICAN JOURL OF MEDICAL GENETICS, 1990
SUP-HD1 - A NEW HODGKINS DISEASE-DERIVED CELL-LINE WITH LYMPHOID FEATURES PRODUCES INTERFERON-GAMMA
BLOOD, 1989
REDUCED NEUTROPHIL COUNTS IN CHILDREN WITH TRANSIENT ERYTHROBLASTOPENIA OF CHILDHOOD
JOURL OF PEDIATRICS, 1989
FAMILIAL BONE-MARROW MONOSOMY
JOURL OF CLINICAL INVESTIGATION, 1989
HEMOGLOBIN FM-FORT-RIPLEY - ANOTHER LESSON FROM THE NEOTE
PEDIATRICS, 1989
HB F-M-OSAKA OR ALPHA-2G-GAMMA-263(E7)HIS-]TYR IN A CAUCASIAN MALE INFANT
HEMOGLOBIN, 1989
TRANSIENT ERYTHROBLASTOPENIA OF CHILDHOOD
WESTERN JOURL OF MEDICINE, 1988
PHILADELPHIA CHROMOSOME-POSITIVE ACUTE LYMPHOBLASTIC
CANCER RESEARCH, 1988
CLINICAL AND BIOLOGIC CHARACTERIZATION OF T-CELL NEOPLASIAS WITH REARRANGEMENTS OF CHROMOSOME
BLOOD, 1988
ELEVATED RED-CELL ADENOSINE
BRITISH JOURL OF HAEMATOLOGY, 1988
Diagnosis and magement of red cell aplasia in children.
Hematology/oncology clinics of North America, 1987
ESTABLISHMENT AND CHARACTERIZATION OF A COMMON ACUTE LYMPHOBLASTIC-LEUKEMIA CELL
CANCER RESEARCH, 1987
TRANSIENT ERYTHROBLASTOPENIA OF ADOLESCENCE
CLINICAL PEDIATRICS, 1986
PYRUVATE-KISE DEFICIENCY IN DOG AND HUMAN
AMERICAN JOURL OF HEMATOLOGY, 1986
PREDNISONE STIMULATION OF ERYTHROPOIESIS IN LEUKEMIC CHILDREN DURING REMISSION
AMERICAN JOURL OF HEMATOLOGY, 1986
COMPARATIVE ACTIVITY OF ERYTHROCYTE ADENOSINE-DEAMISE AND OROTIDINE DECARBOXYLASE IN DIAMOND
AMERICAN JOURL OF HEMATOLOGY, 1986
SCREENING FOR ANEMIA AND ERYTHROCYTE DISORDERS IN CHILDREN
PEDIATRICS, 1986
CHRONIC INFECTIOUS-MONONUCLEOSIS SYNDROME, PANCYTOPENIA
AMERICAN JOURL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 1986
PANCYTOPENIA WITH MYELOFIBROSIS - AN UNUSUAL PRESENTATION OF CHILDHOOD HODGKINS-DISEASE
CLINICAL PEDIATRICS, 1986
MONO-VALENT CATION CHANGES IN SICKLE ERYTHROCYTES - A DIRECT REFLECTION OF ALPHA-GLOBIN GENE NUMBER
JOURL OF LABORATORY AND CLINICAL MEDICINE, 1985
CHILDHOOD BONE-MARROW MONOSOMY-7 SYNDROME - A FAMILIAL DISORDER
JOURL OF PEDIATRICS, 1985
FATAL MYOCARDIAL-INFARCTION FOLLOWING THERAPY WITH PROTHROMBIN COMPLEX CONCENTRATES IN A YOUNG MAN
PEDIATRICS, 1984
IMMUNE THROMBOCYTOPENIA ASSOCIATED WITH ACUTE NONLYMPHOCYTIC LEUKEMIA
JOURL OF PEDIATRICS, 1984
MONOCLOL-ANTIBODY AND ENZYMATIC PROFILES OF HUMAN-MALIGNT LYMPHOID-T CELLS AND DERIVED CELL-LINES
CANCER RESEARCH, 1984
ACUTE NONLYMPHOCYTIC LEUKEMIA DEVELOPING DURING THE COURSE OF EWINGS-SARCOMA
MEDICAL AND PEDIATRIC ONCOLOGY, 1984
COMPARATIVE MONO-VALENT CATION-TRANSPORT IN NEOTAL AND ADULT RED-BLOOD-CELLS
PEDIATRIC RESEARCH, 1984
ELEVATED ERYTHROCYTE ADENOSINE-DEAMISE ACTIVITY IN CONGENITAL HYPOPLASTIC-ANEMIA
NEW ENGLAND JOURL OF MEDICINE, 1983
PLATELET-ASSOCIATED IMMUNOGLOBULIN-G IN CHILDHOOD IDIOPATHIC THROMBOCYTOPENIC PURPURA
JOURL OF PEDIATRICS, 1983
THE RED-BLOOD-CELL AS A BIOPSY TOOL
CLINICS IN HAEMATOLOGY, 1981
ERYTHROCYTE ENZYME DISORDERS IN CHILDREN
PEDIATRIC CLINICS OF NORTH AMERICA, 1980
HEREDITARY SPHEROCYTOSIS
PEDIATRIC ANLS, 1980
Erythrocyte disorders leading to potassium loss and cellular dehydration.
Progress in clinical and biological research, 1979
MICROCYTOSIS ASSOCIATED WITH SICKLE-CELL ANEMIA
AMERICAN JOURL OF CLINICAL PATHOLOGY, 1979
EOSINOPHILIA IN CHILDREN
PEDIATRIC ANLS, 1979
LEUKOCYTE COUNTS IN CHILDREN WITH SICKLE-CELL DISEASE - COMPARATIVE VALUES IN STEADY-STATE
AMERICAN JOURL OF DISEASES OF CHILDREN, 1978
RED-BLOOD-CELL SIZE AND GLYCOLYTIC ENZYME-ACTIVITY
PEDIATRIC RESEARCH, 1978
ENERGY RESERVE AND CATION COMPOSITION OF IRREVERSIBLY SICKLED CELLS INVIVO
BRITISH JOURL OF HAEMATOLOGY, 1978
CATION PERMEABILITY ALTERATIONS DURING SICKLING
BLOOD, 1978
HEMOLYTIC DISORDERS OF INFANCY
CLINICS IN HAEMATOLOGY, 1978
PHYSIOLOGIC FEATURES OF HEMOLYSIS ASSOCIATED WITH ALTERED CATION AND 2,3-DIPHOSPHOGLYCERATE CONTENT
BLOOD, 1978
CATION SPECIFICITY OF PROPRANOLOL-INDUCED CHANGES IN RBC MEMBRANE
JOURL OF CELLULAR PHYSIOLOGY, 1977
BENIGN COURSE OF EXTREME HYPERBILIRUBINEMIA IN SICKLE-CELL ANEMIA - ALYSIS OF 6 CASES
JOURL OF PEDIATRICS, 1977
Care of the critically ill child: the bleeding neote.
Pediatrics, 1976
EVALUATION OF HEMOLYTIC ROLE OF ASPIRIN IN GLUCOSE-6-PHOSPHATE-DEHYDROGESE DEFICIENCY
JOURL OF PEDIATRICS, 1976
SALICYLATE-INDUCED INJURY OF PYRUVATE-KISE-DEFICIENT ERYTHROCYTES
NEW ENGLAND JOURL OF MEDICINE, 1976
ENERGY METABOLISM IN HUMAN ERYTHROCYTES - ROLE OF PHOSPHOGLYCERATE KISE IN CATION-TRANSPORT
BLOOD, 1975
INVIVO HEPATIC AND INTESTIL TOXICITY OF SODIUM CYATE IN RATS - CYATE
JOURL OF LABORATORY AND CLINICAL MEDICINE, 1975
ROLE OF ELEVATED GLUCOSE CONCENTRATIONS IN HEMOLYSIS OF GLUCOSE-6
PROCEEDINGS OF THE SOCIETY FOR EXPERIMENTAL BIOLOGY AND MEDICINE, 1975
HEMOLYSIS DUE TO PYRUVATE-KISE DEFICIENCY AND OTHER GLYCOLYTIC ENZYMOPATHIES
CLINICS IN HAEMATOLOGY, 1975
CONGENITAL HEMOLYTIC-ANEMIA ASSOCIATED WITH DEHYDRATED ERYTHROCYTES AND INCREASED POTASSIUM LOSS
NEW ENGLAND JOURL OF MEDICINE, 1974
ONCOR VIRUS DISEASE - SYNDROME OF HEMOLYTIC-ANEMIA AND LYMPH-NODE CYSTIC-DISEASE
LABORATORY INVESTIGATION, 1974
EFFECT OF CYATE ON ERYTHROCYTE DEFORMABILITY
BLOOD, 1974
CONGENITAL HEMOLYTIC-ANEMIA WITH POTASSIUM LOSS - REPLY
NEW ENGLAND JOURL OF MEDICINE, 1974
EFFECT OF CYATE ON ERYTHROCYTE-MEMBRANE SURFACE CHARGE
PROCEEDINGS OF THE SOCIETY FOR EXPERIMENTAL BIOLOGY AND MEDICINE, 1973
INTRAVASCULAR HEMOLYSIS ASSOCIATED WITH INTRAVENOUS UREA INFUSIONS IN NORMAL INDIVIDUALS
BLOOD, 1973
HEMOLYSIS BY DIPHENYLSULFONES - COMPARATIVE EFFECTS OF DDS AND HYDROXYLAMINE-DDS
JOURL OF LABORATORY AND CLINICAL MEDICINE, 1973
DECREASED GLUTATHIONE PEROXIDASE IN NEOTAL ERTHYROCYTES - LACK OF RELATION TO HYDROGEN
PEDIATRIC RESEARCH, 1972
CYATE INHIBITION OF ERYTHROCYTE GLUCOSE-6-PHOSPHATE DEHYDROGESE
TURE, 1972
MECHANISM OF METHEMOGLOBIN FORMATION BY DIPHENYLSULFONES - EFFECT OF 4
BIOCHEMICAL PHARMACOLOGY, 1972
EFFECT OF COBALT UPON IRON ABSORPTION
PROCEEDINGS OF THE SOCIETY FOR EXPERIMENTAL BIOLOGY AND MEDICINE, 1970
Observations on the effect of testosterone and hydrocortisone on erythropoiesis.
Anls of the New York Academy of Sciences, 1968
OBSERVATIONS ON EFFECT OF TESTOSTERONE AND HYDROCORTISONE ON ERYTHROPOIESIS
ANLS OF THE NEW YORK ACADEMY OF SCIENCES, 1968
ROLE OF CELLULAR PI IN PI TRANSPORT AND METABOLISM IN HUMAN RED CELLS
BIOCHIMICA ET BIOPHYSICA ACTA, 1968
PHOSPHATE RELEASE FROM HUMAN ERYTHROCYTES
BIOCHIMICA ET BIOPHYSICA ACTA, 1968
2,4-DINITROPHENOL INHIBITION OF P32 RELEASE FROM HUMAN RED CELLS
EXPERIENTIA, 1968
What is Dr. Glader's NPI number?An National Provider Identifier (NPI) is a unique ID number that identifies doctors and healthcare providers nationwide.
Dr. Glader's National Provider Identifier (NPI) number is 1417082272.
What common questions do patients ask about Dr. Glader?
Here are answers to patients Frequently Asked Questions (FAQ’s) about Dr. Glader
What is Dr. Bertil Glader's specialty?
Dr. Glader is a Pediatric Hematologist-Oncologist near Palo Alto, CA. A pediatrician trained in the integration of pediatrics, hematology, and oncology, specializing in the recognition and management of blood disorders and cancer in children. This expert provides comprehensive care for conditions such as anemia, bleeding disorders, and various pediatric cancers. Contact Dr. Glader to book an appointment today.
Is this Dr. Bertil Glader affiliated with a ranked Castle Connolly Top Hospital?
Yes, Dr. Glader is affiliated with Stanford Health Care - Stanford Hospital which is a Castle Connolly Top Hospital. Castle Connolly Top Hospitals are healthcare institutions recognized for their excellence in specific medical procedures and overall patient care. They are identified through a rigorous peer nomination process, evaluating factors like patient outcomes, quality of care, and expertise. The list recognizes hospitals that excel in 20 or more specific medical procedures, representing the top 25% nationwide. Castle Connolly Top Hospitals
Where can I learn more about Pediatric Hematologist-Oncologist?
Explore Pediatric Hematologist-Oncologist with insights from trusted medical experts on EverydayHealth.com, where you'll find the most relevant content and helpful condition guides for up-to date information about symptoms, causes, diagnosis, treatment and more. See all our health guides to find trusted information on medical conditions from our experts at Everyday Health.
Is Bertil Glader accepting new patients in Palo Alto, CA?
Yes, Dr. Bertil Glader is accepting new patients at this time.
Does Dr. Bertil Glader offer online booking?
Please contact Dr. Glader's office at (650) 497-8000 for information about online booking, telehealth, or to schedule an appointment.
How can I make an appointment with Bertil Glader?
Please contact Dr. Glader's office at (650) 497-8000 for information regarding telehealth appointment availability or for scheduling assistance.
Which board certifications does Dr. Bertil Glader have?
Dr. Bertil Glader is certified by the American Board of Pediatrics.
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