MARIA NEW, M.D.
Medical Practice at Gustave L Levy Pl, New York, NY

License number

New York 077040

Personal information

See more information about MARIA NEW at radaris.com

Name

Address

Phone

Maria New, age 94

460 E 79Th St APT 16D, New York, NY 10075

Maria New

East Hampton, NY

(631) 267-9734

Maria I New

525 68Th St, New York, NY 10021

(212) 746-3458
(212) 746-3450

Maria I New

525 68Th St, New York, NY 10021

(212) 746-3458
(212) 746-3450

Maria New

5 98 At South Street Via, New York, NY 10001

(212) 241-8210

Organization information

See more information about MARIA NEW at bizstanding.com

Maria New MD

525 E 68 St, New York, NY 10065

Industry:

Pediatric Endocrinologist, Pediatrician

Phone:

(212) 746-3456 (Phone)

Maria Iandolo New

Professional information

See more information about MARIA NEW at trustoria.com

Maria I. New, New York NY

Specialties:

Endocrinologist, Pediatric Endocrinologist, Pediatrician

Address:

5 East 98Th Street, 10Th Floor, New York, NY 10029

Education:

Medical School - University of Pennsylvania, MD
New York Presbyterian Hospital (Residency - Pediatrics)
Bellevue Hospital (Internship - Internal Medicine)
New York Presbyterian - Weill Cornell Medical Center (Fellowship - Pediatrics)
Cornell University (Degree: B.A. )

Languages:

English, Spanish, Italian

Awards and Publications:

New MI, Wilson RC. Steroid disorders in children: congenital adrenal hyperplasia and apparent mineralocorticoid excess. . Proc Natl Acad Sci 1999.; 96:: 12790-12797., Lin-Su K, Zhou P, Arora N, Betensky B, New MI, Wilson RC. In Vitro Expression Studies Of A Novel Mutation ?299 In A Patient Affected With Apparent Mineralocorticoid Excess (AME). . J Clin Endocrinol Metab. 2004; 89: 2024-2027., Nimkarn S, Lin-Su K, New MI, Wilson R, Berglind N. Aldosterone-to-Renin Ratio as a Marker for Disease Severity in 21-Hydroxylase Congenital Adrenal Hyperplasia. J Clin Endo Metab 2007 January; 92(1): 137-142., Wilson RC, Nimkarn S, Dumic M, New MI, Azar M, Najmabadi H, Saffari F, Obeid J. Ethnic Specific Distribution of Mutations in 716 Patients with Congenital Adrenal Hyperplasia Owing to 21-Hydroxylase Deficiency. Mol Genet Metab 2007 Jan; E-Pub ., Trinh L, Lin-Su K, New MI, Nimkarn S. Growth and pubertal characteristics in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. J Ped Endocrinol Metab;., New MI. Extensive Personal Experience: Nonclassical 21-Hydroxylase Deficiency. J Clin Endo Metab 2006; 91: 4222-4231., Meyer-Bahlburg HL, Dolezal C, New MI, Kessler SJ, Schober JM, Zucker KJ. The Recalled Gender Questionnaire-Revised: A Psychometric Analysis in a Sample of Women with Congenital Adrenal Hyperplasia. J Sex Res 2006; 43(4): 364-367., Bhangoo A, Ten S, New MI, Wilson R. Donor splice mutation in the 11?-hydroxylase (CYP11B1) gene resulting in sex reversal: a case report and review of the literature. J Pediatr Endrocinol Metab 2006; 19: 1267-1282., Ergun-Longmire B, Auchus R, New MI, Tansil S, Wilson RC, Papri-Zareei M. Two novel mutations found in a patient with 17?-hydroxylase deficiency. J Clin Endocrinol Metab 2006; 91(10): 4179-4182., Meyer-Bahlburg HF, Dolezal C, New MI, Ehrhardt AA, Baker SW. Gender Development in Women with Congenital Adrenal Hyperplasia as a Function of Disorder Severity. Arch Sex Behav 2006; 35: 667-684., Ergun-Longmire B, Vinci G, Alonso L, New MI, Lin-Su K, McElreavey K, Tansil S. Clinical, hormonal and cytogenetic evaluation of 46,XX males and review of the literature. J Pediatr Endocrinol Metab 2005; 23(8): 739-748., Lin-Su K, Vogiatzi MG, Marshall I, New MI, Macapagal MC, Betensky B, Tansil S, Harbison MD. Treatment with Growth Hormone and LHRH Analogue Improves Final Adult Height in Children with Congenital Adrenal Hyperplasia. J Clin Endocrinol Metab 2005; 90: 3318-3325.

Board certifications:

American Board of Pediatrics

Professor Of Pediatrics And Genetics At Mount Sinai School Of Medicine

Position:

Professor of Pediatrics and Genetics at Mount Sinai School of Medicine

Location:

Greater New York City Area

Industry:

Research

Work:

Mount Sinai School of Medicine - Professor of Pediatrics and Genetics

Teacher At Nyc Dept Of Education

Location:

Greater New York City Area

Industry:

Education Management

Lost Mitigation Dept At Coldwell Banker Liberty

Location:

Greater New York City Area

Industry:

Real Estate

Maria Iandolo New, New York NY

Specialties:

Pediatrics, Pediatric Endocrinology, Endocrinology, Diabetes & Metabolism

Work:

Mt Sinai Hospital
1 Gustave L Levy Pl, New York, NY 10029

Education:

University of Pennsylvania(1954)

Dr. Maria New, New York NY - MD (Doctor of Medicine)

Specialties:

Pediatrics

Address:

MT SINAI SCHOOL OF MEDICINE
1 Gustave L Levy Pl SUITE 1200, New York 10029
(212) 831-4393 (Phone), (212) 426-7627 (Fax)
MOUNT SINAI SCHOOL OF MEDICINE
1 Gustave L Levy Pl SUITE 1198, New York 10029
(212) 241-9464 (Phone), (212) 289-8569 (Fax)
Mount Sinai Pediatrics
5 E 98Th St SUITE 1198, New York 10029
(212) 241-8210 (Phone)
DEPALO, LOUIS R, M.D.
5 E 98Th St SUITE 10TH, New York 10029
(212) 241-6585 (Phone), (212) 987-7259 (Fax)

Certifications:

Pediatrics, 1960

Awards:

Healthgrades Honor Roll

Languages:

English, Italian

Education:

Medical School
Perelman School of Medicine University of Pennsylvania
Graduated: 1954
Bellevue Hospital Center
New York Hospital

Method For Determining Steroids In Human Body Liquids

US Patent:

4431743, Feb 14, 1984

Filed:

Oct 28, 1980

Appl. No.:

6/201589

Inventors:

Songja Pang - New York NY
Maria New - New York NY

Assignee:

Cornell Research Foundation, Inc. - Ithaca NY

International Classification:

G01N 3356, G01N 3358, G01N 3360, G01N 3352

US Classification:

436542

Abstract:

A method for determination of a steroid such as dehydroepiandrosterone sulfate (DS) in a sample of a human body liquid wherein the liquid sample is transferred to a sheet of microfilter paper and dried before being treated with an aqueous solvent to obtain a mixture wherein the dried body liquid is substantially redissolved in the aqueous solution. The mixture is contacted with an aqueous solution of an agent capable of selectively binding the steroid in the presence of a radioisotopically labeled form of steriod whereby part of the labeled steroid and part of the unlabeled steroid present in the sample are bound by forming a complex with the binding agent. Bound steroids are separated from unbound steroids in the aqueous solution and the radioactivity of at least the separated binding agent-steroids-complex or the unbound steroids is performed to determine the concentration of the hormone as a function of measured radioactivity. Additionally, a means for performing the method is disclosed.

Method For Determining Steroids In Human Body Liquids

US Patent:

4230684, Oct 28, 1980

Filed:

Mar 16, 1978

Appl. No.:

5/887326

Inventors:

Songja Pang - New York NY
Maria I. New - New York NY

Assignee:

Cornell Research Foundation, Inc. - Ithaca NY

International Classification:

A61K 4300, G01N 3316, B65D 8132

US Classification:

424 1

Abstract:

A micromethod for the determination of steroids in human body liquids, in particular blood, is disclosed. A small sample of the liquid is transferred to a sheet of absorbing material, e. g. , filter paper. A disc of the impregnated paper, containing the dried sample, in eluted with an aqueous solvent, e. g. , a buffer solution. Without separating the paper from the elute, the latter is extracted with an organic solvent. A steroid-containing residue is recovered from the organic extract and is subjected to a conventional radioimmunoassay. The method is particularly suited for the detection of disorders with elevated steroid levels such as congenital adrenal hyperplasia in newborn infants by determining the 17. alpha. -hydroxy-progesterone concentration in small blood samples.

Genetic Probe Used In The Detection Of Adrenal Hyperplasia

US Patent:

4720454, Jan 19, 1988

Filed:

Apr 18, 1984

Appl. No.:

6/601650

Inventors:

Perrin C. White - Bronx NY
Bo Dupont - Harrison NY
Maria I. New - New York NY

International Classification:

C12Q 168, C12N 1500

US Classification:

435 6

Abstract:

A cDNA clone is isolated encoding a bovine adrenal cytochrome P-450 specific for steroid 21-hydroxylation (P-450. sub. C21). This plasmid pC21a contains an insert of 520 base pairs. It hybridizes with mRNA encoding P-450. sub. C21. The peptide encoded by the insert is highly homologous to two peptides isolated from porcine P-450. sub. C21 and shows limited homology to the P-450 induced by phenobarbital in rat liver. This probe and its human equivalents can be used to screen in utero i. e. pre-natal as well as post-natal patients for adrenal hyperplasia since it reacts well with human DNA as shown. These probes can also be useful for an industrial fermentation process to produce cortisone in quantity.