Manmohan Memorial Institute of Health Sciences - The Edu Fair Nepal
David Foster Foundation Summer 2021 Newsletter by David Foster Foundation - Issuu
Team MMIHS Merchandise Custom Ink Fundraising
NORD Announces over $100,000 in Grant Funding Available for Rare Disease Research
Team MMIHS Merchandise Custom Ink Fundraising
The MMIHS Foundation, Inc. | Nonprofit organization
Zane's Diagnostic Odyssey: His Mother's Story in Honor of Undiagnosed Day - National Organization for Rare Disorders
NORD and the Galactosemia Foundation Jointly Publish First “Voice of the Patient” Report to Help Inform the FDA and Researchers - National Organization for Rare Disorders
What Does MMIHS Look Like? – MMIHS
MMIHS – Megacystis Microcolon Intestinal Hypoperistalsis Syndrome
Ava Gets Support For Her Rare GI Condition - Children's Health
2022 MMIHS Day – MMIHS
What is MMIHS? – MMIHS
MMIHS DAY! – Attitude & Intestinal Fortitude
Unexpected discovery offers rare disease hope - SVI
The MMIHS Foundation | LinkedIn
Fundraiser by Sarah Turman : Ava's $10 for 10th birthday fundraiser for MMIHS
The MMIHS Foundation, Inc. | Nonprofit organization
The MMIHS Foundation – MMIHS
Malaya Gohn - Fundraising For Children's Miracle Network at Penn State Hershey Children's Hospital
BU Research Blog | Erasmus+ exchange visit to Nepal by Dr. Rebecca Neal | Bournemouth University
Heterozygous De Novo and Inherited Mutations in the Smooth Muscle Actin (ACTG2) Gene Underlie Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome | PLOS Genetics
Hats off to MMIHS! Custom Ink Fundraising
MMIHS – Megacystis Microcolon Intestinal Hypoperistalsis Syndrome
BU Research Blog | My experience of the Turing student mobility programme in Nepal | Bournemouth University
