Alison G. May

Internal Medicine
780 Albany St
Boston, MA 02118

Last Updated: 09/26/2026

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Found 8 publications

Home Visiting: Improving Children's and Families' Well-Being.

Home Visiting: Improving Children's and Families' Well-Being.

Journal: NCSL legisbrief
Published: September 11, 2018

A recurring mutation in the respiratory complex 1 protein NDUFB11 is responsible for a novel form of X-linked sideroblastic anemia.

A recurring mutation in the respiratory complex 1 protein NDUFB11 is responsible for a novel form of X-linked sideroblastic anemia.

Journal: Blood
Published: May 27, 2016

Congenital sideroblastic anemia due to mutations in the mitochondrial HSP70 homologue HSPA9.

Congenital sideroblastic anemia due to mutations in the mitochondrial HSP70 homologue HSPA9.

Journal: Blood
Published: September 14, 2015

EMQN Best Practice Guidelines for molecular and haematology methods for carrier identification and prenatal diagnosis of the haemoglobinopathies.

EMQN Best Practice Guidelines for molecular and haematology methods for carrier identification and prenatal diagnosis of the haemoglobinopathies.

Journal: European journal of human genetics : EJHG
Published: March 13, 2015

Mutations in TRNT1 cause congenital sideroblastic anemia with immunodeficiency, fevers, and developmental delay (SIFD).

Mutations in TRNT1 cause congenital sideroblastic anemia with immunodeficiency, fevers, and developmental delay (SIFD).

Journal: Blood
Published: September 07, 2014

EMQN Best Practice Guidelines for molecular and haematology methods for carrier identification and prenatal diagnosis of the haemoglobinopathies.

EMQN Best Practice Guidelines for molecular and haematology methods for carrier identification and prenatal diagnosis of the haemoglobinopathies.

Journal: European journal of human genetics : EJHG
Published: February 22, 2014

X-linked sideroblastic anemia due to ALAS2 intron 1 enhancer element GATA-binding site mutations.

X-linked sideroblastic anemia due to ALAS2 intron 1 enhancer element GATA-binding site mutations.

Journal: American journal of hematology
Published: October 20, 2013

A novel syndrome of congenital sideroblastic anemia, B-cell immunodeficiency, periodic fevers, and developmental delay (SIFD).

A novel syndrome of congenital sideroblastic anemia, B-cell immunodeficiency, periodic fevers, and developmental delay (SIFD).

Journal: Blood
Published: April 05, 2013
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Last Updated: 09/26/2026